FDA Application
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NDC Search Results on Active Ingredient: ibuprofen
Click on Active Ingredient to view the label.
Ingredient Name | NDC | Company Name | Application Number or Regulatory Citation | Product Type | Marketing Category |
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IBUPROFEN; HYDROCODONE BITARTRATE | 53746-117-01 | Amneal Pharmaceuticals of New York LLC | ANDA076642 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN; HYDROCODONE BITARTRATE | 53746-146-01 | Amneal Pharmaceuticals of New York LLC | ANDA076642 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN; HYDROCODONE BITARTRATE | 33261-378-02 | Aidarex Pharmaceuticals LLC | ANDA076604 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN; MECLIZINE HYDROCHLORIDE; LOPERAMIDE HYDROCHLORIDE; DIMETHICONE; DOXYLAMINE SUCCINATE | 72663-205-48 | Welly Health PBC | part336 | HUMAN OTC DRUG | OTC monograph not final |
IBUPROFEN; METHYL SALICYLATE; MENTHOL; CAPSAICIN | 70859-030-01 | NuCare Pharmaceuticals,Inc. | ANDA075682 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE | 50580-436-01 | Johnson & Johnson Consumer Inc. | ANDA203200 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE | 41163-158-46 | United Natural Foods, Inc. dba UNFI | ANDA203200 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE | 41163-158-60 | United Natural Foods, Inc. dba UNFI | ANDA203200 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE | 37808-158-60 | H E B | ANDA203200 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; POLYMYXIN B SULFATE; HYDROCORTISONE; BACITRACIN ZINC; NEOMYCIN SULFATE | 72663-151-44 | Welly Health PBC | part348 | HUMAN OTC DRUG | OTC monograph not final |
IBUPROFEN; PRASTERONE | 55607-400-10 | Health Science Funding, LLC | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE | 58602-803-13 | Aurohealth LLC | ANDA209235 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE | 58602-803-79 | Aurohealth LLC | ANDA209235 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE | 0573-0180-21 | Haleon US Holdings LLC | NDA019771 | HUMAN OTC DRUG | NDA |
IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE | 51660-493-41 | Ohm Laboratories Inc. | ANDA074567 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE | 37808-423-40 | HEB | ANDA074567 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE | 21130-423-41 | Safeway Inc. | ANDA074567 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE | 11673-423-41 | Target Corporation | ANDA074567 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE | 51660-490-41 | Ohm Laboratories Inc. | ANDA074567 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE | 58602-803-67 | Aurohealth LLC | ANDA209235 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE | 0363-0423-21 | WALGREEN COMPANY | ANDA074567 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE | 62011-0070-1 | Strategic Sourcing Services LLC | ANDA074567 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE | 59779-430-41 | CVS Pharmacy | ANDA074567 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE | 70000-0606-1 | Cardinal Health | ANDA209235 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE | 58602-803-08 | Aurohealth LLC | ANDA209235 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE | 0363-0423-41 | WALGREEN COMPANY | ANDA074567 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE | 36800-423-21 | Topco Associates LLC | ANDA074567 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE | 46122-609-58 | Amerisource Bergen | ANDA209235 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE | 11822-0084-6 | Rite-Aid | ANDA074567 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE | 58602-803-83 | Aurohealth LLC | ANDA209235 | HUMAN OTC DRUG | ANDA |
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