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 | 59556-895-50 | Strides Pharma Inc | ANDA204469 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 59556-895-79 | Strides Pharma Inc | ANDA204469 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 59556-895-85 | Strides Pharma Inc | ANDA204469 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 59556-895-86 | Strides Pharma Inc | ANDA204469 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 59556-895-87 | Strides Pharma Inc | ANDA204469 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 59556-895-88 | Strides Pharma Inc | ANDA204469 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 59651-032-12 | Aurobindo Pharma Limited | ANDA209178 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 59651-032-47 | Aurobindo Pharma Limited | ANDA209178 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 59651-360-01 | Aurobindo Pharma Limited | ANDA213794 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 59651-360-05 | Aurobindo Pharma Limited | ANDA213794 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 59651-361-01 | Aurobindo Pharma Limited | ANDA213794 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 59651-361-05 | Aurobindo Pharma Limited | ANDA213794 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 59651-362-01 | Aurobindo Pharma Limited | ANDA213794 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 59651-362-05 | Aurobindo Pharma Limited | ANDA213794 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 59726-046-16 | P & L Development, LLC | ANDA207753 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 59726-046-20 | P & L Development, LLC | ANDA207753 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 59726-046-30 | P & L Development, LLC | ANDA207753 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 59726-123-16 | P & L Development, LLC | ANDA202300 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 59726-199-10 | P & L Development, LLC | ANDA078682 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 59726-199-16 | P & L Development, LLC | ANDA078682 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 59726-199-20 | P & L Development, LLC | ANDA078682 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 59726-661-40 | P & L Development, LLC | ANDA079174 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 59726-661-50 | P & L Development, LLC | ANDA079174 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 59726-745-10 | P & L Development, LLC | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 59726-745-16 | P & L Development, LLC | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 59726-745-20 | P & L Development, LLC | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 59726-745-40 | P & L Development, LLC | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 59726-843-10 | P & L Development, LLC | ANDA206568 | HUMAN OTC DRUG | ANDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 59779-050-27 | CVS Pharmacy | ANDA079113 | HUMAN OTC DRUG | ANDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 59779-050-33 | CVS Pharmacy | ANDA079113 | HUMAN OTC DRUG | ANDA |
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