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 | 0573-0179-20 | GlaxoSmithKline Consumer Healthcare Holdings (US) LLC | NDA020944 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0191-75 | GlaxoSmithKline Consumer Healthcare Holdings (US) LLC | NDA020812 | HUMAN OTC DRUG | NDA |
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 | 72657-157-36 | GLENMARK THERAPEUTICS INC., USA | ANDA218311 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; IBUPROFEN | 72657-157-76 | 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 | 72657-157-05 | GLENMARK THERAPEUTICS INC., USA | ANDA218311 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; IBUPROFEN | 72657-157-18 | GLENMARK THERAPEUTICS INC., USA | ANDA218311 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 82501-1582-1 | Gobrands, Inc | ANDA079129 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 51407-370-05 | Golden State Medical Supply, Inc. | ANDA075682 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 51407-369-05 | Golden State Medical Supply, Inc. | ANDA075682 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 51407-371-05 | Golden State Medical Supply, Inc. | ANDA075682 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 50804-199-40 | Good Sense (Geiss, Destin & Dunn, Inc.) | ANDA078682 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50804-750-20 | Good Sense (Geiss, Destin & Dunn, Inc.) | ANDA206999 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50804-199-20 | Good Sense (Geiss, Destin & Dunn, Inc.) | ANDA078682 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50804-750-40 | Good Sense (Geiss, Destin & Dunn, Inc.) | ANDA206999 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 62207-365-25 | Granules India Limited | BULK INGREDIENT | Export only | |
IBUPROFEN | 62207-395-43 | Granules India Limited | ANDA079174 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 62207-395-46 | Granules India Limited | ANDA079174 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 62207-396-46 | Granules India Limited | ANDA079174 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 62207-358-42 | Granules India Limited | ANDA202312 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 62207-303-13 | Granules India Limited | BULK INGREDIENT | Export only | |
IBUPROFEN | 62207-355-47 | Granules India Limited | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 62207-366-51 | Granules India Limited | ANDA079174 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 62207-395-51 | Granules India Limited | ANDA079174 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 62207-358-49 | Granules India Limited | ANDA202312 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 62207-396-42 | Granules India Limited | ANDA079174 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 62207-366-46 | Granules India Limited | ANDA079174 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 62207-358-47 | Granules India Limited | ANDA202312 | HUMAN OTC DRUG | ANDA |
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