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 | 67296-1611-3 | RedPharm Drug, Inc. | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 67296-1633-3 | RedPharm Drug, Inc. | ANDA202413 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 67296-1634-3 | RedPharm Drug, Inc. | ANDA202413 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; IBUPROFEN | 67296-1655-7 | RedPharm Drug, Inc. | ANDA204575 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 67296-1685-2 | RedPharm Drug, Inc. | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 67296-1685-3 | RedPharm Drug, Inc. | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 67296-1686-1 | RedPharm Drug, Inc. | ANDA078329 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 67296-1686-3 | RedPharm Drug, Inc. | ANDA078329 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 67296-1706-3 | RedPharm Drug, Inc. | ANDA078329 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 67296-1716-3 | RedPharm Drug, Inc. | ANDA078329 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 67296-1717-3 | RedPharm Drug, Inc. | ANDA075682 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 67296-1756-1 | RedPharm Drug, Inc. | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 67296-1756-3 | RedPharm Drug, Inc. | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 67296-1757-1 | RedPharm Drug, Inc. | ANDA078329 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 67296-1757-3 | RedPharm Drug, Inc. | ANDA078329 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 67296-1799-3 | RedPharm Drug, Inc. | ANDA078558 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 67296-1800-3 | RedPharm Drug, Inc. | ANDA078558 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 67296-1912-3 | Redpharm Drug | ANDA078558 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 67414-240-00 | Jones Healthcare Group - Packaging Services, Inc | ANDA077349 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 67414-240-09 | Jones Healthcare Group - Packaging Services, Inc | ANDA077349 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 67751-120-01 | Navajo Manufacturing Company Inc. | NDA019012 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 67751-120-02 | Navajo Manufacturing Company Inc. | NDA019012 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 67751-146-01 | Navajo Manufacturing Company Inc. | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 67751-146-02 | Navajo Manufacturing Company Inc. | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 67751-146-03 | Navajo Manufacturing Company Inc. | NDA018989 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 67751-147-01 | Navajo Manufacturing Company Inc. | NDA021394 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 67751-147-02 | Navajo Manufacturing Company Inc. | NDA021394 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 67751-148-01 | Navajo Manufacturing Company Inc. | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 67751-148-02 | Navajo Manufacturing Company Inc. | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 67751-148-03 | Navajo Manufacturing Company Inc. | NDA020402 | HUMAN OTC DRUG | NDA |
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