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 | 50580-409-20 | Johnson & Johnson Consumer Inc. | ANDA078682 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50580-409-80 | Johnson & Johnson Consumer Inc. | ANDA078682 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE | 50580-436-01 | Johnson & Johnson Consumer Inc. | ANDA203200 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; DIPHENHYDRAMINE CITRATE | 50580-563-20 | Johnson & Johnson Consumer Inc. | ANDA079113 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; DIPHENHYDRAMINE CITRATE | 50580-563-40 | Johnson & Johnson Consumer Inc. | ANDA079113 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; DIPHENHYDRAMINE CITRATE | 50580-563-80 | Johnson & Johnson Consumer Inc. | ANDA079113 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50580-601-04 | Johnson & Johnson Consumer Inc. | NDA020516 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 50580-601-08 | Johnson & Johnson Consumer Inc. | NDA020516 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 50580-601-20 | Johnson & Johnson Consumer Inc. | NDA020516 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 50580-601-21 | Johnson & Johnson Consumer Inc. | NDA020516 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 50580-601-22 | Johnson & Johnson Consumer Inc. | NDA020516 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 50580-601-25 | Johnson & Johnson Consumer Inc. | NDA020516 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 50580-603-04 | Johnson & Johnson Consumer Inc. | NDA020516 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 50580-604-04 | Johnson & Johnson Consumer Inc. | NDA020516 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 50580-932-01 | Johnson & Johnson Consumer Inc. | ANDA076359 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50580-933-01 | Johnson & Johnson Consumer Inc. | ANDA076359 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50594-005-78 | Big Lots Stores, Inc. | ANDA077349 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50594-018-26 | Big Lots Stores, Inc. | ANDA074937 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50594-020-76 | Big Lots Stores, Inc. | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50594-146-04 | BIG LOTS STORES, INC. | ANDA206999 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50594-843-20 | Big Lots | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50804-199-20 | Good Sense (Geiss, Destin & Dunn, Inc.) | ANDA078682 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50804-199-40 | Good Sense (Geiss, Destin & Dunn, Inc.) | ANDA078682 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50804-750-20 | Good Sense (Geiss, Destin & Dunn, Inc.) | ANDA206999 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50804-750-40 | Good Sense (Geiss, Destin & Dunn, Inc.) | ANDA206999 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50844-257-15 | L.N.K. International, Inc. | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50844-291-01 | L.N.K. International, Inc. | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50844-291-02 | L.N.K. International, Inc. | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50844-291-03 | L.N.K. International, Inc. | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50844-291-08 | L.N.K. International, Inc. | ANDA075010 | HUMAN OTC DRUG | ANDA |
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