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 | 41250-647-78 | Meijer Distribution Inc | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41250-647-82 | Meijer Distribution Inc | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41250-647-90 | Meijer Distribution Inc | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41250-660-26 | Meijer Distribution Inc | ANDA074937 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41250-685-26 | Meijer Distribution Inc | ANDA074937 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41250-685-34 | Meijer Distribution Inc | ANDA074937 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41250-726-62 | Meijer Distribution Inc | ANDA076359 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41250-752-16 | MEIJER, INC. | ANDA206999 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41250-752-30 | MEIJER, INC. | ANDA206999 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41250-752-40 | MEIJER, INC. | ANDA206999 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41250-752-80 | MEIJER, INC. | ANDA206999 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41250-897-26 | Meijer Distribution Inc | ANDA074937 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41250-897-28 | Meijer Distribution Inc | ANDA074937 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41250-897-34 | Meijer Distribution Inc | ANDA074937 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41250-991-03 | Meijer Distribution Inc | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41250-993-12 | Meijer Distribution Inc | ANDA075139 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41250-993-20 | Meijer Distribution Inc | ANDA075139 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41250-993-91 | Meijer Distribution Inc | ANDA075139 | HUMAN OTC DRUG | ANDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 41520-050-27 | American Sales Company | ANDA079113 | HUMAN OTC DRUG | ANDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 41520-050-48 | American Sales Company | ANDA079113 | HUMAN OTC DRUG | ANDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 41520-050-58 | American Sales Company | ANDA079113 | HUMAN OTC DRUG | ANDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 41520-050-60 | American Sales Company | ANDA079113 | HUMAN OTC DRUG | ANDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 41520-050-76 | American Sales Company | ANDA079113 | HUMAN OTC DRUG | ANDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 41520-050-82 | American Sales Company | ANDA079113 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41520-057-05 | American Sales Company | ANDA075217 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41520-166-26 | American Sales Company | ANDA074937 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41520-166-28 | American Sales Company | ANDA074937 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41520-255-10 | American Sales Company | ANDA075217 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; DIPHENHYDRAMINE CITRATE | 41520-413-27 | American Sales Company | ANDA079113 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; DIPHENHYDRAMINE CITRATE | 41520-413-60 | American Sales Company | ANDA079113 | HUMAN OTC DRUG | ANDA |
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