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 | 37808-221-20 | H E B | ANDA202300 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 37808-750-30 | H E B | ANDA206999 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 37808-699-40 | H E B | ANDA078682 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 37808-750-20 | H E B | ANDA206999 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 37808-604-62 | H E B | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 37808-393-13 | H E B | ANDA075139 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 37808-393-12 | H E B | ANDA075139 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 37808-604-71 | H E B | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 37808-363-26 | H E B | ANDA074937 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 37808-699-20 | H E B | ANDA078682 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 37808-647-71 | H E B | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 37808-604-85 | H E B | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 37808-221-40 | H E B | ANDA202300 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 37808-897-26 | H E B | ANDA074937 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 37808-699-80 | H E B | ANDA078682 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 37808-255-10 | H E B | ANDA075217 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 37808-647-90 | H E B | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 37808-393-20 | H E B | ANDA075139 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 37808-699-30 | H E B | ANDA078682 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 37808-709-71 | H E B | ANDA077349 | HUMAN OTC DRUG | ANDA |
PHENYLEPHRINE HYDROCHLORIDE; IBUPROFEN | 37808-158-60 | H E B | ANDA203200 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 37808-200-26 | H E B | ANDA074937 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 37808-921-08 | H E B | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 37808-750-80 | H E B | ANDA206999 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 37808-922-13 | H E B | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 37808-221-80 | H E B | ANDA202300 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 52959-076-15 | H.J. Harkins Company Inc. dba Pharma Pac | ANDA078558 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 52959-075-20 | H.J. Harkins Company Inc. dba Pharma Pac | ANDA078558 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 52959-187-50 | H.J. Harkins Company Inc. dba Pharma Pac | part343 | HUMAN OTC DRUG | OTC MONOGRAPH NOT FINAL |
IBUPROFEN | 52959-077-24 | H.J. Harkins Company Inc. dba Pharma Pac | ANDA078558 | HUMAN PRESCRIPTION DRUG | ANDA |
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