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 | 53345-039-02 | Humanwell PuraCap Pharmaceutical (Wuhan) Co., Ltd | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 62936-0941-1 | INGLES MARKETS, INC. | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 62936-0941-5 | INGLES MARKETS, INC. | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 59105-002-10 | J.P BUSINESS ENTERPRISE | ANDA079205 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50269-157-03 | JC World Bell Wholesale Co., Inc. | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 50269-157-02 | JC World Bell Wholesale Co., Inc. | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 50269-000-01 | JC World Bell Wholesale Co., Inc. | ANDA077349 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50269-000-25 | JC World Bell Wholesale Co., Inc. | ANDA077349 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50269-157-01 | JC World Bell Wholesale Co., Inc. | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 73598-1102-1 | JHK Inc dba American Safety & First Aid | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 73598-1104-1 | JHK Inc dba American Safety & First Aid | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50580-230-04 | Johnson & Johnson Consumer Inc. | ANDA077349 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50580-230-03 | Johnson & Johnson Consumer Inc. | ANDA077349 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50580-601-08 | Johnson & Johnson Consumer Inc. | NDA020516 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 50580-601-21 | Johnson & Johnson Consumer Inc. | NDA020516 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 50580-604-04 | Johnson & Johnson Consumer Inc. | NDA020516 | HUMAN OTC DRUG | NDA |
ACETAMINOPHEN; IBUPROFEN | 50580-208-16 | Johnson & Johnson Consumer Inc. | ANDA214836 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50580-120-20 | Johnson & Johnson Consumer Inc. | ANDA078682 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; IBUPROFEN | 50580-208-02 | Johnson & Johnson Consumer Inc. | ANDA214836 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50580-230-01 | Johnson & Johnson Consumer Inc. | ANDA077349 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50580-409-80 | Johnson & Johnson Consumer Inc. | ANDA078682 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50580-100-18 | Johnson & Johnson Consumer Inc. | NDA020603 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 50580-932-01 | Johnson & Johnson Consumer Inc. | ANDA076359 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50580-120-80 | Johnson & Johnson Consumer Inc. | ANDA078682 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50580-198-51 | Johnson & Johnson Consumer Inc. | NDA020603 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 50580-198-50 | Johnson & Johnson Consumer Inc. | NDA020603 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 50580-230-09 | Johnson & Johnson Consumer Inc. | ANDA077349 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50580-230-05 | Johnson & Johnson Consumer Inc. | ANDA077349 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; DIPHENHYDRAMINE CITRATE | 50580-563-20 | Johnson & Johnson Consumer Inc. | ANDA079113 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50580-603-04 | Johnson & Johnson Consumer Inc. | NDA020516 | HUMAN OTC DRUG | NDA |
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