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 |
---|---|---|---|---|---|
IBUPROFEN | 60687-468-11 | American Health Packaging | ANDA078558 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 60687-468-01 | American Health Packaging | ANDA078558 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 60687-743-46 | American Health Packaging | ANDA210602 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 60687-446-11 | American Health Packaging | ANDA078558 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 60687-743-40 | American Health Packaging | ANDA210602 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; HYDROCODONE BITARTRATE | 68084-841-01 | American Health Packaging | ANDA076642 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 41520-521-62 | American Sales Company | ANDA076359 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41520-897-26 | American Sales Company | ANDA074937 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41520-647-76 | American Sales Company | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41520-604-85 | American Sales Company | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41520-604-76 | American Sales Company | ANDA072096 | HUMAN OTC DRUG | ANDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 41520-050-27 | American Sales Company | ANDA079113 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41520-057-05 | American Sales Company | ANDA075217 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41520-604-62 | American Sales Company | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41520-604-71 | American Sales Company | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41520-647-78 | American Sales Company | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41520-604-90 | American Sales Company | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41520-647-90 | American Sales Company | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41520-166-26 | American Sales Company | ANDA074937 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41520-647-71 | American Sales Company | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41520-604-82 | American Sales Company | ANDA072096 | 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 | 41520-897-34 | American Sales Company | ANDA074937 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41520-660-28 | American Sales Company | ANDA074937 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41520-660-26 | American Sales Company | ANDA074937 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41520-633-62 | American Sales Company | ANDA076359 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41520-685-26 | American Sales Company | ANDA074937 | HUMAN OTC DRUG | ANDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 41520-050-76 | American Sales Company | ANDA079113 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; DIPHENHYDRAMINE CITRATE | 41520-413-60 | American Sales Company | ANDA079113 | HUMAN OTC DRUG | ANDA |
-