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 | 50844-291-10 | L.N.K. International, Inc. | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50844-291-11 | L.N.K. International, Inc. | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50844-291-12 | L.N.K. International, Inc. | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50844-291-13 | L.N.K. International, Inc. | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50844-291-14 | L.N.K. International, Inc. | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50844-291-15 | L.N.K. International, Inc. | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50844-291-16 | L.N.K. International, Inc. | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50844-291-17 | L.N.K. International, Inc. | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50844-291-29 | L.N.K. International, Inc. | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50844-291-99 | L.N.K. International, Inc. | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50844-292-00 | L.N.K. International, Inc. | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50844-292-01 | L.N.K. International, Inc. | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50844-292-02 | L.N.K. International, Inc. | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50844-292-08 | L.N.K. International, Inc. | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50844-292-11 | L.N.K. International, Inc. | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50844-292-12 | L.N.K. International, Inc. | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50844-292-13 | L.N.K. International, Inc. | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50844-292-14 | L.N.K. International, Inc. | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50844-292-15 | L.N.K. International, Inc. | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50844-292-16 | L.N.K. International, Inc. | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50844-352-02 | L.N.K. International, Inc. | ANDA075139 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50844-352-12 | L.N.K. International, Inc. | ANDA075139 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50844-352-15 | L.N.K. International, Inc. | ANDA075139 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50844-352-16 | L.N.K. International, Inc. | ANDA075139 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50844-353-02 | L.N.K. International, Inc. | ANDA075139 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50844-353-16 | L.N.K. International, Inc. | ANDA075139 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50844-392-02 | L.N.K. International, Inc. | ANDA075139 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50844-392-08 | L.N.K. International, Inc. | ANDA075139 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50844-392-12 | L.N.K. International, Inc. | ANDA075139 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50844-392-14 | L.N.K. International, Inc. | ANDA075139 | HUMAN OTC DRUG | ANDA |
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