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 | 68071-4009-9 | NuCare Pharmaceuticals,Inc. | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 68071-3053-2 | NuCare Pharmaceuticals,Inc. | ANDA075682 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 68071-2903-4 | NuCare Pharmaceuticals,Inc. | ANDA213794 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 68071-2903-7 | NuCare Pharmaceuticals,Inc. | ANDA213794 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 68071-4217-4 | NuCare Pharmaceuticals,Inc. | ANDA074916 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 68071-1628-4 | NuCare Pharmaceuticals,Inc. | ANDA210602 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 68071-2739-1 | NuCare Pharmaceuticals,Inc. | ANDA071268 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 68071-4009-7 | NuCare Pharmaceuticals,Inc. | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 68071-2942-4 | NuCare Pharmaceuticals,Inc. | ANDA076925 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 68071-2903-5 | NuCare Pharmaceuticals,Inc. | ANDA213794 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 68071-3442-3 | NuCare Pharmaceuticals,Inc. | ANDA213794 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 68071-3362-3 | NuCare Pharmaceuticals,Inc. | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 68071-3125-9 | NuCare Pharmaceuticals,Inc. | ANDA075682 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 68071-3172-4 | NuCare Pharmaceuticals,Inc. | ANDA075682 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 68071-2759-6 | NuCare Pharmaceuticals,Inc. | ANDA071268 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 68071-3053-4 | NuCare Pharmaceuticals,Inc. | ANDA075682 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 68071-5134-6 | NuCare Pharmaceuticals,Inc. | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE | 51660-493-41 | Ohm Laboratories Inc. | ANDA074567 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE | 51660-423-41 | Ohm Laboratories Inc. | ANDA074567 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE | 51660-423-21 | Ohm Laboratories Inc. | ANDA074567 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE | 51660-490-41 | Ohm Laboratories Inc. | ANDA074567 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 69729-157-10 | OPMX LLC | ANDA079174 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 70253-199-40 | OUR FAMILY (Nash Finch Company) | ANDA078682 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 70253-199-80 | OUR FAMILY (Nash Finch Company) | ANDA078682 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 70253-199-20 | OUR FAMILY (Nash Finch Company) | ANDA078682 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 59726-661-50 | P & L Development, LLC | ANDA079174 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 59726-046-16 | P & L Development, LLC | ANDA207753 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 59726-046-20 | P & L Development, LLC | ANDA207753 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 59726-199-10 | P & L Development, LLC | ANDA078682 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 59726-843-10 | P & L Development, LLC | ANDA206568 | HUMAN OTC DRUG | ANDA |
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