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 | 72789-364-10 | PD-Rx Pharmaceuticals, Inc. | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 72789-364-15 | PD-Rx Pharmaceuticals, Inc. | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 72789-364-20 | PD-Rx Pharmaceuticals, Inc. | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 72789-364-21 | PD-Rx Pharmaceuticals, Inc. | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 72789-364-30 | PD-Rx Pharmaceuticals, Inc. | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 72789-364-40 | PD-Rx Pharmaceuticals, Inc. | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 72789-364-60 | PD-Rx Pharmaceuticals, Inc. | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 72789-364-90 | PD-Rx Pharmaceuticals, Inc. | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 72789-364-93 | PD-Rx Pharmaceuticals, Inc. | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 72789-382-30 | PD-Rx Pharmaceuticals, Inc. | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 72865-132-16 | XLCare Pharmaceuticals, Inc | ANDA206999 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 72865-132-20 | XLCare Pharmaceuticals, Inc | ANDA206999 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 72865-132-40 | XLCare Pharmaceuticals, Inc | ANDA206999 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 72865-132-80 | XLCare Pharmaceuticals, Inc | ANDA206999 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 72927-805-01 | Strides Consumer LLC | ANDA207052 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 72927-805-02 | Strides Consumer LLC | ANDA207052 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; CIMETIDINE; SALICYLIC ACID | 72934-1047-2 | Sincerus Florida, LLC | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
TERBINAFINE; FLUCONAZOLE; ITRACONAZOLE; IBUPROFEN | 72934-4176-9 | Sincerus Florida, LLC | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
IBUPROFEN | 73086-210-01 | SKYA HEALTH, LLC | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 73086-211-01 | SKYA HEALTH, LLC | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 73086-212-01 | SKYA HEALTH, LLC | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 73097-008-02 | Savings Distributors LLC | NDA019012 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 73097-008-40 | Savings Distributors LLC | NDA019012 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 73097-008-50 | Savings Distributors LLC | NDA019012 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 73408-509-33 | Thompson Safety | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 73408-809-33 | Thompson Safety | ANDA079174 | HUMAN OTC DRUG | ANDA |
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 | 73659-012-01 | Rapid Care, Inc. | ANDA079174 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 73659-012-02 | Rapid Care, Inc. | ANDA079174 | HUMAN OTC DRUG | ANDA |
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