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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TERBINAFINE; FLUCONAZOLE; IBUPROFEN; ITRACONAZOLE | 72934-4176-9 | Sincerus Florida, LLC | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
WATER; ACETAMINOPHEN; IBUPROFEN; HYDROCORTISONE; POLYMYXIN B SULFATE; ALCOHOL; BACITRACIN ZINC; NEOMYCIN SULFATE; DIPHENHYDRAMINE HYDROCHLORIDE; ISOPROPYL ALCOHOL | 51142-002-01 | ASO LLC | 505G(a)(3) | HUMAN OTC DRUG | OTC Monograph Drug |
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