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 | 51013-421-15 | PuraCap Pharmaceutical LLC | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 51013-103-26 | PuraCap Pharmaceutical LLC | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 51013-422-39 | PuraCap Pharmaceutical LLC | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 51013-103-42 | PuraCap Pharmaceutical LLC | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 51013-103-63 | PuraCap Pharmaceutical LLC | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 51013-103-22 | PuraCap Pharmaceutical LLC | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 51013-103-25 | PuraCap Pharmaceutical LLC | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 51013-421-25 | PuraCap Pharmaceutical LLC | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 51013-103-15 | PuraCap Pharmaceutical LLC | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 51013-103-41 | PuraCap Pharmaceutical LLC | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 51013-405-26 | PuraCap Pharmaceutical LLC | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 51013-319-54 | PuraCap Pharmaceutical LLC | ANDA079174 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 51013-103-38 | PuraCap Pharmaceutical LLC | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 51013-410-26 | PuraCap Pharmaceutical LLC | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 51013-429-26 | PURACAP PHARMACEUTICAL LLC | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 51013-405-25 | PuraCap Pharmaceutical LLC | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 51013-421-26 | PuraCap Pharmaceutical LLC | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 51013-103-28 | PuraCap Pharmaceutical LLC | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 51013-103-39 | PuraCap Pharmaceutical LLC | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 51013-103-31 | PuraCap Pharmaceutical LLC | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 59088-756-00 | PureTek Corporation | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
IBUPROFEN | 83474-002-04 | Puro Pharma Inc. | ANDA210602 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 42708-175-30 | QPharma Inc | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 42708-097-30 | QPharma Inc | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 42708-057-60 | QPharma Inc | ANDA078558 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 42708-097-60 | QPharma Inc | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 55700-445-40 | Quality Care Products LLC | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 55700-446-00 | Quality Care Products LLC | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 55700-446-90 | Quality Care Products LLC | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 55700-445-30 | Quality Care Products LLC | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
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