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 | 72476-843-16 | Care One (Retail Business Services, LLC.) | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 72476-843-20 | Care One (Retail Business Services, LLC.) | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 72476-843-40 | Care One (Retail Business Services, LLC.) | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 72476-745-80 | Care One (Retail Business Services, LLC.) | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 72476-745-18 | Care One (Retail Business Services, LLC.) | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 76413-344-01 | Central Texas Community Health Centers | ANDA074916 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 76413-313-24 | Central Texas Community Health Centers | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 76413-312-15 | Central Texas Community Health Centers | ANDA075217 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 76413-345-01 | Central Texas Community Health Centers | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 68016-633-50 | Chain Drug Consortium | ANDA075139 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 68016-634-50 | Chain Drug Consortium | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 68016-633-24 | Chain Drug Consortium | ANDA075139 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 68016-635-10 | Chain Drug Consortium | ANDA075139 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 68016-634-10 | Chain Drug Consortium | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 68016-635-50 | Chain Drug Consortium | ANDA075139 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 68016-633-10 | Chain Drug Consortium | ANDA075139 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 68016-634-24 | Chain Drug Consortium | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 68016-645-08 | Chain Drug Consortium | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 68016-634-25 | Chain Drug Consortium | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 68016-634-00 | Chain Drug Consortium | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 68016-634-05 | Chain Drug Consortium | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 68016-645-12 | Chain Drug Consortium | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 68016-645-15 | Chain Drug Consortium | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 68016-295-01 | Chain Drug Consortium LLC | ANDA091237 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 68016-295-50 | Chain Drug Consortium LLC | ANDA091237 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 68016-940-08 | Chain Drug Consortium, LLC | ANDA074916 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 68016-943-04 | Chain Drug Consortium, LLC | ANDA074916 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 68016-942-04 | Chain Drug Consortium, LLC | ANDA074916 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 68016-944-04 | Chain Drug Consortium, LLC | ANDA074916 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 68016-813-40 | Chain Drug Consortium, LLC | ANDA206568 | HUMAN OTC DRUG | ANDA |
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