FDA Application
-
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 |
---|---|---|---|---|---|
IBUPROFEN | 59726-199-16 | P & L Development, LLC | ANDA078682 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 59726-745-10 | P & L Development, LLC | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 59726-199-20 | P & L Development, LLC | ANDA078682 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 59726-745-16 | P & L Development, LLC | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 59726-123-16 | P & L Development, LLC | ANDA202300 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 59726-046-30 | P & L Development, LLC | ANDA207753 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 59726-745-40 | P & L Development, LLC | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 59726-745-20 | P & L Development, LLC | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 59726-661-40 | P & L Development, LLC | ANDA079174 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 45802-897-26 | Padagis Israel Pharmaceuticals Ltd | ANDA074937 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 45802-952-26 | Padagis Israel Pharmaceuticals Ltd | ANDA076925 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 45802-057-05 | Padagis Israel Pharmaceuticals Ltd | ANDA075217 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 45802-140-26 | Padagis Israel Pharmaceuticals Ltd | ANDA074937 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 45802-897-34 | Padagis Israel Pharmaceuticals Ltd | ANDA074937 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 45802-952-43 | Padagis Israel Pharmaceuticals Ltd | ANDA076925 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 45802-133-26 | Padagis Israel Pharmaceuticals Ltd | ANDA074937 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 0121-1022-00 | PAI Holdings, LLC dba PAI Pharma | ANDA210602 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 0121-1022-05 | PAI Holdings, LLC dba PAI Pharma | ANDA210602 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 0121-2044-10 | PAI Holdings, LLC dba PAI Pharma | ANDA210602 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 0121-2044-00 | PAI Holdings, LLC dba PAI Pharma | ANDA210602 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 72789-200-21 | PD-Rx Pharmaceuticals, Inc. | ANDA078329 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 72789-187-60 | PD-Rx Pharmaceuticals, Inc. | ANDA078329 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 72789-212-20 | PD-Rx Pharmaceuticals, Inc. | ANDA078329 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 72789-363-20 | PD-Rx Pharmaceuticals, Inc. | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 72789-363-21 | PD-Rx Pharmaceuticals, Inc. | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 43063-867-60 | PD-Rx Pharmaceuticals, Inc. | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 43063-352-06 | PD-Rx Pharmaceuticals, Inc. | ANDA078558 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 72789-364-10 | PD-Rx Pharmaceuticals, Inc. | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 72789-212-06 | PD-Rx Pharmaceuticals, Inc. | ANDA078329 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 43063-845-40 | PD-Rx Pharmaceuticals, Inc. | ANDA078558 | HUMAN PRESCRIPTION DRUG | ANDA |
-