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 |
---|---|---|---|---|---|
GLUCOSAMINE SULFATE; IBUPROFEN; CHONDROITIN SULFATE (BOVINE) | 61841-152-72 | Bayer HealthCare LLC. | HUMAN OTC DRUG | Export only | |
IBUPROFEN | 61919-123-30 | DIRECT RX | part343 | HUMAN OTC DRUG | OTC monograph not final |
IBUPROFEN | 61919-124-30 | Direct Rx | ANDA078558 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 61919-125-30 | Direct Rx | ANDA078558 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 61919-126-30 | Direct Rx | ANDA078558 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 61919-126-60 | Direct Rx | ANDA078558 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 61919-126-72 | Direct Rx | ANDA078558 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 61919-126-90 | Direct Rx | ANDA078558 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; IBUPROFEN | 61919-296-30 | DIRECT RX | ANDA077723 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 61919-463-21 | Direct_Rx | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 61919-463-30 | DIRECT RX | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 61919-463-40 | Direct_Rx | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 61919-463-45 | Direct_Rx | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 61919-463-60 | Direct_Rx | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 61919-463-71 | Direct_Rx | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 61919-463-72 | Direct_Rx | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 61919-463-90 | Direct_Rx | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 61919-621-71 | DIRECT RX | ANDA075682 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 61919-628-21 | Direct_Rx | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 61919-628-30 | DIRECT RX | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 61919-628-60 | Direct_Rx | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 61919-628-90 | Direct_Rx | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 61919-683-30 | Direct_Rx | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 61919-683-60 | Direct_Rx | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 61919-683-90 | Direct_Rx | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 61919-960-21 | Direct_Rx | ANDA075682 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 61919-960-30 | DirectRX | ANDA075682 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 61919-960-60 | Direct_Rx | ANDA075682 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 61919-960-72 | Direct_Rx | ANDA075682 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 61919-960-90 | DirectRX | ANDA075682 | HUMAN PRESCRIPTION DRUG | ANDA |
-