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 | 50332-0152-7 | HART Health | M | HUMAN OTC DRUG | OTC Monograph Drug |
IBUPROFEN | 50332-0152-8 | HART Health | M | HUMAN OTC DRUG | OTC Monograph Drug |
IBUPROFEN | 50436-0319-1 | Unit Dose Services | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 50436-0319-6 | Unit Dose Services | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 50436-0319-7 | Unit Dose Services | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 50436-0321-1 | Unit Dose Services | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 50436-0321-2 | Unit Dose Services | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 50436-0321-3 | Unit Dose Services | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 50436-0321-4 | Unit Dose Services | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 50436-0321-5 | Unit Dose Services | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 50436-0321-6 | Unit Dose Services | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 50436-0323-1 | UNIT DOSE SERVICES | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 50436-0323-2 | UNIT DOSE SERVICES | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 50436-0323-3 | UNIT DOSE SERVICES | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 50436-0684-1 | Unit Dose Services | ANDA075682 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 50436-0684-2 | Unit Dose Services | ANDA075682 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 50436-0684-3 | Unit Dose Services | ANDA075682 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 50436-0684-4 | Unit Dose Services | ANDA075682 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 50436-0684-5 | Unit Dose Services | ANDA075682 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 50436-0684-6 | Unit Dose Services | ANDA075682 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 50436-3200-1 | Unit Dose Services | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 50436-3200-2 | Unit Dose Services | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 50436-3200-3 | Unit Dose Services | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 50436-4604-0 | Unit Dose Services | ANDA075682 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 50436-4604-1 | Unit Dose Services | ANDA075682 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 50436-4604-6 | Unit Dose Services | ANDA075682 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 50436-4605-1 | Unit Dose Services | ANDA075682 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 50436-4605-2 | Unit Dose Services | ANDA075682 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 50436-4605-3 | Unit Dose Services | ANDA075682 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 50436-4606-1 | Unit Dose Services | ANDA078558 | HUMAN PRESCRIPTION DRUG | ANDA |
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