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 | 71309-111-30 | Safrel Pharmaceuticals, LLC. | ANDA079174 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 62207-365-68 | Granules India Limited | BULK INGREDIENT | Export only | |
IBUPROFEN | 68788-8278-2 | Preferred Pharmaceuticals Inc. | ANDA071268 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 68788-8354-7 | Preferred Pharmaceuticals Inc. | ANDA213794 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 68788-9110-6 | Preferred Pharmaceuticals, Inc. | ANDA075682 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 47682-600-13 | Unifirst First Aid Corporation | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 59779-604-71 | CVS Pharmacy | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50090-5160-8 | A-S Medication Solutions | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 54348-825-00 | PharmPak, Inc. | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 68016-634-10 | Chain Drug Consortium | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 11822-4258-6 | RITE AID CORPORATION | ANDA207753 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 53217-366-30 | Aidarex Pharmaceuticals LLC | ANDA075682 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 36800-647-78 | Topco Associates LLC | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN LYSINE | 66993-490-36 | Prasco Laboratories | NDA021903 | HUMAN PRESCRIPTION DRUG | NDA AUTHORIZED GENERIC |
IBUPROFEN LYSINE | 39822-1030-1 | XGen Pharmaceuticals DJB, Inc. | ANDA202402 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN LYSINE | 39822-1030-2 | XGen Pharmaceuticals DJB, Inc. | ANDA202402 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN LYSINE | 55292-122-52 | Recordati Rare Diseases Inc. | NDA021903 | HUMAN PRESCRIPTION DRUG | NDA |
IBUPROFEN SODIUM | 0573-0134-80 | Haleon US Holdings LLC | NDA201803 | HUMAN OTC DRUG | NDA |
IBUPROFEN SODIUM | 0573-0133-88 | Haleon US Holdings LLC | NDA201803 | HUMAN OTC DRUG | NDA |
IBUPROFEN SODIUM | 0573-0230-40 | Haleon US Holdings LLC | NDA201803 | HUMAN OTC DRUG | NDA |
IBUPROFEN SODIUM | 0573-0133-20 | Haleon US Holdings LLC | NDA201803 | HUMAN OTC DRUG | NDA |
IBUPROFEN SODIUM | 0573-0133-40 | Haleon US Holdings LLC | NDA201803 | HUMAN OTC DRUG | NDA |
IBUPROFEN SODIUM | 0573-0133-01 | Haleon US Holdings LLC | NDA201803 | HUMAN OTC DRUG | NDA |
IBUPROFEN SODIUM | 0573-0133-05 | Haleon US Holdings LLC | NDA201803 | HUMAN OTC DRUG | NDA |
IBUPROFEN SODIUM | 0573-0133-04 | Haleon US Holdings LLC | NDA201803 | HUMAN OTC DRUG | NDA |
IBUPROFEN SODIUM | 0573-0133-80 | Haleon US Holdings LLC | NDA201803 | HUMAN OTC DRUG | NDA |
IBUPROFEN SODIUM | 0573-0133-41 | Haleon US Holdings LLC | NDA201803 | HUMAN OTC DRUG | NDA |
IBUPROFEN SODIUM | 0573-0230-20 | Haleon US Holdings LLC | NDA201803 | HUMAN OTC DRUG | NDA |
IBUPROFEN SODIUM | 0573-0133-81 | Haleon US Holdings LLC | NDA201803 | HUMAN OTC DRUG | NDA |
IBUPROFEN SODIUM | 0573-0134-20 | Haleon US Holdings LLC | NDA201803 | HUMAN OTC DRUG | NDA |
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