FDA Application
-
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 |
---|---|---|---|---|---|
ACETAMINOPHEN; IBUPROFEN | 72657-157-05 | GLENMARK THERAPEUTICS INC., USA | ANDA218311 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; IBUPROFEN | 72657-157-18 | GLENMARK THERAPEUTICS INC., USA | ANDA218311 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; IBUPROFEN | 72657-157-20 | GLENMARK THERAPEUTICS INC., USA | ANDA218311 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; IBUPROFEN | 72657-157-36 | GLENMARK THERAPEUTICS INC., USA | ANDA218311 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; IBUPROFEN | 72657-157-72 | GLENMARK THERAPEUTICS INC., USA | ANDA218311 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; IBUPROFEN | 72657-157-74 | GLENMARK THERAPEUTICS INC., USA | ANDA218311 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; IBUPROFEN | 72657-157-76 | GLENMARK THERAPEUTICS INC., USA | ANDA218311 | HUMAN OTC DRUG | ANDA |
NEOMYCIN SULFATE; IBUPROFEN; POLYMYXIN B SULFATE; HYDROCORTISONE; BACITRACIN ZINC | 72663-151-44 | Welly Health PBC | part348 | HUMAN OTC DRUG | OTC monograph not final |
IBUPROFEN; HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE; BACITRACIN ZINC | 72663-152-05 | Welly Health PBC | part348 | HUMAN OTC DRUG | OTC monograph not final |
LOPERAMIDE HYDROCHLORIDE; MECLIZINE HYDROCHLORIDE; DIMETHICONE; DOXYLAMINE SUCCINATE; IBUPROFEN | 72663-205-48 | Welly Health PBC | part336 | HUMAN OTC DRUG | OTC monograph not final |
IBUPROFEN | 72789-185-20 | PD-Rx Pharmaceuticals, Inc. | ANDA078329 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 72789-185-30 | PD-Rx Pharmaceuticals, Inc. | ANDA078329 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 72789-185-60 | PD-Rx Pharmaceuticals, Inc. | ANDA078329 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 72789-185-82 | PD-Rx Pharmaceuticals, Inc. | ANDA078329 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 72789-185-90 | PD-Rx Pharmaceuticals, Inc. | ANDA078329 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 72789-186-30 | PD-Rx Pharmaceuticals, Inc. | ANDA078329 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 72789-186-60 | PD-Rx Pharmaceuticals, Inc. | ANDA078329 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 72789-186-82 | PD-Rx Pharmaceuticals, Inc. | ANDA078329 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 72789-186-90 | PD-Rx Pharmaceuticals, Inc. | ANDA078329 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 72789-187-30 | PD-Rx Pharmaceuticals, Inc. | ANDA078329 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 72789-187-60 | PD-Rx Pharmaceuticals, Inc. | ANDA078329 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 72789-187-82 | PD-Rx Pharmaceuticals, Inc. | ANDA078329 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 72789-187-90 | PD-Rx Pharmaceuticals, Inc. | ANDA078329 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 72789-191-20 | PD-Rx Pharmaceuticals, Inc. | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 72789-191-30 | PD-Rx Pharmaceuticals, Inc. | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 72789-198-10 | PD-Rx Pharmaceuticals, Inc. | ANDA078329 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 72789-200-10 | PD-Rx Pharmaceuticals, Inc. | ANDA078329 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 72789-200-12 | PD-Rx Pharmaceuticals, Inc. | ANDA078329 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 72789-200-15 | PD-Rx Pharmaceuticals, Inc. | ANDA078329 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 72789-200-20 | PD-Rx Pharmaceuticals, Inc. | ANDA078329 | HUMAN PRESCRIPTION DRUG | ANDA |
-