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0031-8739 is the Product NDC for ROBITUSSIN MAXIMUM STRENGTH COUGH PLUS CHEST CONGESTION DM (dextromethorphan hydrobromide 20; 400mg/20mL; mg/20mL, guaifenesin 20; 400mg/20mL; mg/20mL solution for oral use) manufactured by Haleon US Holdings LLC. |
0031-8742 is the Product NDC for Robitussin Peak Cold Multi-Symptom Cold (dextromethorphan hydrobromide 10; 100; 5mg/5mL; mg/5mL; mg/5mL, guaifenesin 10; 100; 5mg/5mL; mg/5mL; mg/5mL, and phenylephrine hydrochloride 10; 100; 5mg/5mL; mg/5mL; mg/5mL liquid for oral use) manufactured by Haleon US Holdings LLC. |
0031-8743 is the Product NDC for ROBITUSSIN LONG-ACTING COUGHGELS (dextromethorphan hydrobromide 15mg/1 capsule, liquid filled for oral use) manufactured by Haleon US Holdings LLC. |
0031-8744 is the Product NDC for Robitussin Maximum Strength Severe Multi-Symptom 7 in 1 Relief Nighttime (acetaminophen 325; 15; 6.25mg/1; mg/1; mg/1, dextromethorphan hydrobromide 325; 15; 6.25mg/1; mg/1; mg/1, and doxylamine succinate 325; 15; 6.25mg/1; mg/1; mg/1 capsule, liquid filled for oral use) manufactured by Haleon US Holdings LLC. |
0031-8750 is the Product NDC for Robitussin Maximum Strength Severe Cough Plus Sore Throat (acetaminophen 650; 20mg/20mL; mg/20mL, dextromethorphan hydrobromide 650; 20mg/20mL; mg/20mL liquid for oral use) manufactured by Haleon US Holdings LLC. |
0031-8751 is the Product NDC for Robitussin Severe Multi-Symptom Cough Cold Flu (acetaminophen 650; 20; 400; 10mg/20mL; mg/20mL; mg/20mL; mg/20mL, dextromethorphan hydrobromide 650; 20; 400; 10mg/20mL; mg/20mL; mg/20mL; mg/20mL, guaifenesin 650; 20; 400; 10mg/20mL; mg/20mL; mg/20mL; mg/20mL, phenylephrine hydrochloride 650; 20; 400; 10mg/20mL; mg/20mL; mg/20mL; mg/20mL liquid for oral use) manufactured by Haleon US Holdings LLC. |
0031-8752 is the Product NDC for Robitussin Severe Multi-Symptom Cough Cold Flu Nighttime (acetaminophen 650; 25; 10mg/20mL; mg/20mL; mg/20mL, diphenhydramine hydrochloride 650; 25; 10mg/20mL; mg/20mL; mg/20mL, phenylephrine hydrochloride 650; 25; 10mg/20mL; mg/20mL; mg/20mL solution for oral use) manufactured by Haleon US Holdings LLC. |
0031-8753 is the Product NDC for Robitussin 12 Hour Cough Relief (dextromethorphan polistirex 30mg/5mL suspension, extended release for oral use) manufactured by Haleon US Holdings LLC. |
0031-8754 is the Product NDC for Robitussin 12 Hour Cough Relief (dextromethorphan polistirex 30mg/5mL suspension, extended release for oral use) manufactured by Haleon US Holdings LLC. |
0031-8755 is the Product NDC for Robitussin 12 Hour Cough Relief (dextromethorphan polistirex 30mg/5mL suspension, extended release for oral use) manufactured by Haleon US Holdings LLC. |
0031-8756 is the Product NDC for Robitussin Honey Maximum Strength Cough and Chest Congestion DM (dextromethorphan HBr 20; 400mg/20mL; mg/20mL, guaifenesin 20; 400mg/20mL; mg/20mL solution for oral use) manufactured by Haleon US Holdings LLC. |
0031-8757 is the Product NDC for ROBITUSSIN COUGH PLUS CHEST CONGESTION DM (dextromethorphan hydrobromide and guaifenesin 20; 200mg/20mL; mg/20mL solution for oral use) manufactured by Haleon US Holdings LLC. |
0031-8758 is the Product NDC for Robitussin Honey Maximum Strength Nighttime Cough DM (dextromethorphan HBr 30; 12.5mg/20mL; mg/20mL, doxylamine succinate 30; 12.5mg/20mL; mg/20mL solution for oral use) manufactured by Haleon US Holdings LLC. |
0031-8759 is the Product NDC for Robitussin Sugar-Free Dye-Free Cough Plus Chest Congestion DM (dextromethorphan hydrobromide 20; 200mg/20mL; mg/20mL, guaifenesin 20; 200mg/20mL; mg/20mL solution for oral use) manufactured by Haleon US Holdings LLC. |
0031-8760 is the Product NDC for Childrens Robitussin Honey Cough and Chest Congestion DM (dextromethorphan HBr 10; 100mg/10mL; mg/10mL, guaifenesin 10; 100mg/10mL; mg/10mL solution for oral use) manufactured by Haleon US Holdings LLC. |
0031-8762 is the Product NDC for Childrens Robitussin Honey Nighttime Cough DM (dextromethorphan hbr 15; 6.25mg/10mL; mg/10mL, doxylamine succinate 15; 6.25mg/10mL; mg/10mL solution for oral use) manufactured by Haleon US Holdings LLC. |
0031-8765 is the Product NDC for Robitussin Maximum Strength 12 Hour Cough and Mucus Relief (Dextromethorphan Hydrobromide 60; 1200mg/1; mg/1, Guaifenesin 60; 1200mg/1; mg/1 tablet, extended release for oral use) manufactured by Haleon US Holdings LLC. |
0031-8770 is the Product NDC for Robitussin Honey Severe Cough, Flu Plus Sore Throat Nighttime (acetaminophen and diphenhydramine hydrochloride 650; 25mg/20mL; mg/20mL solution for oral use) manufactured by Haleon US Holdings LLC. |
0031-8771 is the Product NDC for Robitussin Honey Severe Cough, Flu Plus Sore Throat (acetaminophen 650; 20mg/20mL; mg/20mL, dextromethorphan hbr 650; 20mg/20mL; mg/20mL solution for oral use) manufactured by Haleon US Holdings LLC. |
0031-9301 is the Product NDC for Robitussin Direct Sore Throat Pain (acetaminophen 500mg/1 tablet, coated for oral use) manufactured by Haleon US Holdings LLC. |
0031-9302 is the Product NDC for Robitussin Direct Cough (dextromethorphan hydrobromide 15mg/1 capsule, liquid filled for oral use) manufactured by Haleon US Holdings LLC. |
0031-9303 is the Product NDC for Robitussin Direct Chest Congestion (guaifenesin 400mg/1 tablet, coated for oral use) manufactured by Haleon US Holdings LLC. |
0031-9305 is the Product NDC for Robitussin Direct Stuffy Nose (Phenylephrine hcl 10mg/1 tablet, coated for oral use) manufactured by Haleon US Holdings LLC. |
0031-9306 is the Product NDC for Robitussin Medi-Soothers (dextromethorphan hydrobromide 5; 5mg/1; mg/1, menthol 5; 5mg/1; mg/1 lozenge for oral use) manufactured by Haleon US Holdings LLC. |
0031-9307 is the Product NDC for Robitussin Medi-Soothers (dextromethorphan hydrobromide 5; 5mg/1; mg/1, menthol 5; 5mg/1; mg/1 lozenge for oral use) manufactured by Haleon US Holdings LLC. |
0031-9310 is the Product NDC for ROBITUSSIN LONG-ACTING COUGH Soft CHEWS (dextromethorphan hydrobromide 15mg/1 tablet, chewable for oral use) manufactured by Haleon US Holdings LLC. |
0031-9311 is the Product NDC for ROBITUSSIN Nighttime Cough DM Soft CHEWS (dextromethorphan hydrobromide 15; 6.25mg/1; mg/1, doxylamine succinate 15; 6.25mg/1; mg/1 tablet, chewable for oral use) manufactured by Haleon US Holdings LLC. |
0032-0045 is the Product NDC for Creon (Pancrelipase 15000; 3000; 9500[USP'U]/1; [USP'U]/1; [USP'U]/1 capsule, delayed release for oral use) manufactured by AbbVie Inc.. |
0032-0046 is the Product NDC for Creon (Pancrelipase 30000; 6000; 19000[USP'U]/1; [USP'U]/1; [USP'U]/1 capsule, delayed release pellets for oral use) manufactured by AbbVie Inc.. |
0032-0047 is the Product NDC for Creon (Pancrelipase 60000; 12000; 38000[USP'U]/1; [USP'U]/1; [USP'U]/1 capsule, delayed release pellets for oral use) manufactured by AbbVie Inc.. |
0032-1203 is the Product NDC for Creon (Pancrelipase 15000; 3000; 9500[USP'U]/1; [USP'U]/1; [USP'U]/1 capsule, delayed release for oral use) manufactured by AbbVie Inc.. |
0032-1206 is the Product NDC for Creon (Pancrelipase 30000; 6000; 19000[USP'U]/1; [USP'U]/1; [USP'U]/1 capsule, delayed release pellets for oral use) manufactured by AbbVie Inc.. |
0032-1212 is the Product NDC for Creon (Pancrelipase 60000; 12000; 38000[USP'U]/1; [USP'U]/1; [USP'U]/1 capsule, delayed release pellets for oral use) manufactured by AbbVie Inc.. |
0032-1224 is the Product NDC for Creon (Pancrelipase 120000; 24000; 76000[USP'U]/1; [USP'U]/1; [USP'U]/1 capsule, delayed release pellets for oral use) manufactured by AbbVie Inc.. |
0032-2636 is the Product NDC for Creon (Pancrelipase 120000; 24000; 76000[USP'U]/1; [USP'U]/1; [USP'U]/1 capsule, delayed release pellets for oral use) manufactured by AbbVie Inc.. |
0032-2637 is the Product NDC for Creon (Pancrelipase 180000; 36000; 114000[USP'U]/1; [USP'U]/1; [USP'U]/1 capsule, delayed release pellets for oral use) manufactured by AbbVie Inc.. |
0032-3016 is the Product NDC for Creon (Pancrelipase 180000; 36000; 114000[USP'U]/1; [USP'U]/1; [USP'U]/1 capsule, delayed release pellets for oral use) manufactured by AbbVie Inc.. |
0037-0022 is the Product NDC for sfRowasa Sulfite-Free Formulation (mesalamine 4g/60mL suspension for rectal administration) manufactured by Meda Pharmaceuticals Inc.. |
0037-0066 is the Product NDC for Rowasa (mesalamine 4g/60mL suspension for rectal administration) manufactured by Meda Pharmaceuticals Inc.. |
0037-0245 is the Product NDC for DYMISTA (Azelastine Hydrochloride and Fluticasone Propionate 137; 50ug/1; ug/1 spray, metered for nasal administration) manufactured by Meda Pharmaceuticals Inc.. |
0037-0430 is the Product NDC for Felbatol (felbamate 400mg/1 tablet for oral use) manufactured by Meda Pharmaceuticals Inc.. |
0037-0431 is the Product NDC for Felbatol (felbamate 600mg/1 tablet for oral use) manufactured by Meda Pharmaceuticals Inc.. |
0037-0442 is the Product NDC for Felbatol (felbamate 600mg/5mL suspension for oral use) manufactured by Meda Pharmaceuticals Inc.. |
0037-0678 is the Product NDC for Gastrocrom (cromolyn sodium 20mg/mL liquid for oral use) manufactured by Meda Pharmaceuticals. |
0037-2001 is the Product NDC for Soma (Carisoprodol 350mg/1 tablet for oral use) manufactured by Meda Pharmaceuticals Inc.. |
0037-2250 is the Product NDC for Soma (Carisoprodol 250mg/1 tablet for oral use) manufactured by Meda Pharmaceuticals Inc.. |
0037-4401 is the Product NDC for Depen (Penicillamine 250mg/1 tablet for oral use) manufactured by Meda Pharmaceuticals Inc.. |
0037-4801 is the Product NDC for ELESTRIN (ESTRADIOL 0.52mg/.87g gel, metered for topical use) manufactured by Meda Pharmaceuticals Inc.. |
0037-6010 is the Product NDC for Edluar (Zolpidem Tartrate 10mg/1 tablet for oral use) manufactured by Meda Pharmaceuticals Inc.. |
0037-6050 is the Product NDC for Edluar (Zolpidem Tartrate 5mg/1 tablet for oral use) manufactured by Meda Pharmaceuticals Inc.. |
0037-6321 is the Product NDC for URELLE (hyoscyamine sulfate .12; 81; 10.8; 32.4; 40.8mg/1; mg/1; mg/1; mg/1; mg/1, methenamine .12; 81; 10.8; 32.4; 40.8mg/1; mg/1; mg/1; mg/1; mg/1, methylene blue .12; 81; 10.8; 32.4; 40.8mg/1; mg/1; mg/1; mg/1; mg/1, phenyl salicylate .12; 81; 10.8; 32.4; 40.8mg/1; mg/1; mg/1; mg/1; mg/1, and sodium phosphate .12; 81; 10.8; 32.4; 40.8mg/1; mg/1; mg/1; mg/1; mg/1, monobasic .12; 81; 10.8; 32.4; 40.8mg/1; mg/1; mg/1; mg/1; mg/1, monohydrate .12; 81; 10.8; 32.4; 40.8mg/1; mg/1; mg/1; mg/1; mg/1 tablet for oral use) manufactured by Meda Pharmaceuticals. |
0037-6822 is the Product NDC for PROCTOFOAM HC (pramoxine hydrochloride hydrocortisone acetate 100; 100mg/10g; mg/10g aerosol, foam for topical use) manufactured by Meda Pharmaceuticals Inc.. |
0037-6823 is the Product NDC for PROCTOFOAM NS (pramoxine hydrochloride 150mg/15g aerosol, foam for rectal administration) manufactured by Meda Pharmaceuticals Inc.. |
0037-6824 is the Product NDC for EPIFOAM (pramoxine hydrochloride and hydrocortisone acetate 100; 100mg/10g; mg/10g aerosol, foam for topical use) manufactured by Meda Pharmaceuticals Inc.. |
0037-6830 is the Product NDC for Cortifoam (hydrocortisone acetate 1500mg/15g aerosol, foam for topical use) manufactured by Meda Pharmaceuticals Inc.. |
0037-6860 is the Product NDC for Dipentum (olsalazine sodium 250mg/1 capsule, gelatin coated for oral use) manufactured by Meda Pharmaceuticals Inc.. |
0046-0749 is the Product NDC for Premarin (CONJUGATED ESTROGENS 25mg/5mL injection, powder, lyophilized, for solution for intramuscular; intravenous administration) manufactured by Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.. |
0046-0872 is the Product NDC for Premarin Vaginal (conjugated estrogens 0.625mg/g cream for vaginal administration) manufactured by Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.. |
0046-1100 is the Product NDC for Premarin (estrogens 0.3mg/1, conjugated 0.3mg/1 tablet, film coated for oral use) manufactured by Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.. |
0046-1101 is the Product NDC for Premarin (estrogens 0.45mg/1, conjugated 0.45mg/1 tablet, film coated for oral use) manufactured by Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.. |
0046-1102 is the Product NDC for Premarin (estrogens 0.625mg/1, conjugated 0.625mg/1 tablet, film coated for oral use) manufactured by Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.. |
0046-1103 is the Product NDC for Premarin (estrogens 0.9mg/1, conjugated 0.9mg/1 tablet, film coated for oral use) manufactured by Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.. |
0046-1104 is the Product NDC for Premarin (estrogens 1.25mg/1, conjugated 1.25mg/1 tablet, film coated for oral use) manufactured by Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.. |
0046-1105 is the Product NDC for Prempro (conjugated estrogens and medroxyprogesterone acetate .3; 1.5mg/1; mg/1 tablet, sugar coated for oral use) manufactured by Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.. |
0046-1106 is the Product NDC for Prempro (conjugated estrogens and medroxyprogesterone acetate .45; 1.5mg/1; mg/1 tablet, sugar coated for oral use) manufactured by Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.. |
0046-1107 is the Product NDC for Prempro (conjugated estrogens and medroxyprogesterone acetate .625; 2.5mg/1; mg/1 tablet, sugar coated for oral use) manufactured by Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.. |
0046-1108 is the Product NDC for Prempro (conjugated estrogens and medroxyprogesterone acetate .625; 5mg/1; mg/1 tablet, sugar coated for oral use) manufactured by Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.. |
0046-2575 is the Product NDC for Premphase (conjugated estrogens and medroxyprogesterone acetate kit for administration) manufactured by Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.. |
0049-0013 is the Product NDC for UNASYN (ampicillin sodium and sulbactam sodium 1; .5g/1; g/1 injection, powder, for solution for intramuscular; intravenous administration) manufactured by Roerig. |
0049-0014 is the Product NDC for UNASYN (ampicillin sodium and sulbactam sodium 2; 1g/1; g/1 injection, powder, for solution for intramuscular; intravenous administration) manufactured by Roerig. |
0049-0024 is the Product NDC for UNASYN (ampicillin sodium and sulbactam sodium 100; 50mg/mL; mg/mL injection, powder, for solution for intramuscular; intravenous administration) manufactured by Roerig. |
0049-0050 is the Product NDC for Zoloft (sertraline hydrochloride 20mg/mL solution, concentrate for oral use) manufactured by ROERIG. |
0049-0056 is the Product NDC for Geodon (ziprasidone hydrochloride 60mg/1 capsule for oral use) manufactured by ROERIG. |
0049-0058 is the Product NDC for Geodon (ziprasidone hydrochloride 80mg/1 capsule for oral use) manufactured by ROERIG. |
0049-0114 is the Product NDC for ERAXIS (anidulafungin 50mg/15mL injection, powder, lyophilized, for solution for intravenous administration) manufactured by Roerig. |
0049-0116 is the Product NDC for ERAXIS (anidulafungin 100mg/30mL injection, powder, lyophilized, for solution for intravenous administration) manufactured by Roerig. |
0049-0174 is the Product NDC for Glucotrol XL (glipizide 5mg/1 tablet, extended release for oral use) manufactured by Roerig. |
0049-0178 is the Product NDC for Glucotrol XL (glipizide 10mg/1 tablet, extended release for oral use) manufactured by Roerig. |
0049-0352 is the Product NDC for Geodon (ziprasidone 20mg/1 capsule for oral use) manufactured by ROERIG. |
0049-0354 is the Product NDC for Geodon (ziprasidone 40mg/1 capsule for oral use) manufactured by ROERIG. |
0049-0356 is the Product NDC for Geodon (ziprasidone 60mg/1 capsule for oral use) manufactured by ROERIG. |
0049-0358 is the Product NDC for Geodon (ziprasidone 80mg/1 capsule for oral use) manufactured by ROERIG. |
0049-0420 is the Product NDC for Pfizerpen (penicillin G potassium 5000000[iU]/1 powder, for solution for intramuscular; intrapleural; intrathecal; intravenous administration) manufactured by Roerig. |
0049-0430 is the Product NDC for Pfizerpen (penicillin G potassium 20000000[iU]/1 powder, for solution for intravenous administration) manufactured by Roerig. |
0049-0520 is the Product NDC for Pfizerpen (penicillin G potassium 5000000[iU]/1 powder, for solution for intramuscular; intrapleural; intrathecal; intravenous administration) manufactured by Roerig. |
0049-0520 is the Product NDC for Pfizerpen (penicillin G potassium 5000000[iU]/1 powder, for solution for intramuscular; intrapleural; intrathecal; intravenous administration) manufactured by Roerig. |
0049-0530 is the Product NDC for Pfizerpen (penicillin G potassium 20000000[iU]/1 powder, for solution for intravenous administration) manufactured by Roerig. |
0049-0530 is the Product NDC for Pfizerpen (penicillin G potassium 20000000[iU]/1 powder, for solution for intravenous administration) manufactured by Roerig. |
0049-2040 is the Product NDC for Cardura XL (doxazosin 4mg/1 tablet, multilayer, extended release for oral use) manufactured by Roerig. |
0049-2080 is the Product NDC for Cardura XL (doxazosin 8mg/1 tablet, multilayer, extended release for oral use) manufactured by Roerig. |
0049-2242 is the Product NDC for ERAXIS (anidulafungin 100mg/30mL injection, powder, lyophilized, for solution for intravenous administration) manufactured by Roerig. |
0049-2330 is the Product NDC for Relpax (eletriptan hydrobromide 20mg/1 tablet, film coated for oral use) manufactured by ROERIG. |
0049-2340 is the Product NDC for Relpax (eletriptan hydrobromide 40mg/1 tablet, film coated for oral use) manufactured by ROERIG. |
0049-2410 is the Product NDC for Cardura (doxazosin 1mg/1 tablet for oral use) manufactured by ROERIG. |
0049-2512 is the Product NDC for Cardura (doxazosin 2mg/1 tablet for oral use) manufactured by ROERIG. |
0049-2614 is the Product NDC for Cardura (doxazosin 4mg/1 tablet for oral use) manufactured by ROERIG. |
0049-2716 is the Product NDC for Cardura (doxazosin 8mg/1 tablet for oral use) manufactured by ROERIG. |
0049-3160 is the Product NDC for VFEND (voriconazole 40mg/mL powder, for suspension for oral use) manufactured by Roerig. |
0049-3170 is the Product NDC for VFEND (voriconazole 50mg/1 tablet, film coated for oral use) manufactured by Roerig. |
0049-3180 is the Product NDC for VFEND (voriconazole 200mg/1 tablet, film coated for oral use) manufactured by Roerig. |
Subsets and Splits