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 | 67877-321-05 | Ascend Laboratories, LLC | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 67877-321-30 | Ascend Laboratories, LLC | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 67877-321-50 | Ascend Laboratories, LLC | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN; FAMOTIDINE | 67877-626-01 | Ascend Laboratories, LLC | ANDA211890 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN; FAMOTIDINE | 67877-626-05 | Ascend Laboratories, LLC | ANDA211890 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN; FAMOTIDINE | 67877-626-06 | Ascend Laboratories, LLC | ANDA211890 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN; FAMOTIDINE | 67877-626-90 | Ascend Laboratories, LLC | ANDA211890 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 68001-435-92 | BluePoint Laboratories | ANDA209179 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 68001-435-94 | BluePoint Laboratories | ANDA209179 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 68001-521-92 | BluePoint Laboratories | ANDA209179 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 68001-521-94 | BluePoint Laboratories | ANDA209179 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; DIPHENHYDRAMINE HYDROCHLORIDE | 68016-057-40 | Premier Value Alliance LLC | ANDA090397 | 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 |
PSEUDOEPHEDRINE HYDROCHLORIDE; IBUPROFEN | 68016-423-21 | Chain Drug Consortium, LLC. | ANDA074567 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 68016-633-10 | Chain Drug Consortium | ANDA075139 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 68016-633-24 | Chain Drug Consortium | ANDA075139 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 68016-633-50 | Chain Drug Consortium | ANDA075139 | 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 | 68016-634-10 | Chain Drug Consortium | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 68016-634-24 | Chain Drug Consortium | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 68016-634-25 | Chain Drug Consortium | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 68016-634-50 | Chain Drug Consortium | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 68016-635-10 | Chain Drug Consortium | ANDA075139 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 68016-635-50 | Chain Drug Consortium | ANDA075139 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 68016-645-08 | 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 | 68016-813-40 | Chain Drug Consortium, LLC | ANDA206568 | HUMAN OTC DRUG | ANDA |
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