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 | 59556-895-48 | Strides Pharma Inc | ANDA204469 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 11673-850-80 | TARGET Corporation | ANDA206999 | HUMAN OTC DRUG | ANDA |
DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN | 0573-0167-42 | Haleon US Holdings LLC | NDA021393 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 49035-647-82 | Wal-Mart Stores Inc | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 0113-4501-27 | L. Perrigo Company | ANDA203599 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50090-3408-0 | A-S Medication Solutions | ANDA074937 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 80267-604-78 | Live Betr LLC | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 11822-0255-1 | Rite Aid Corporation | ANDA075217 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; DIPHENHYDRAMINE CITRATE | 21130-228-73 | Better Living Brands, LLC | ANDA216204 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 36800-604-71 | Topco Associates LLC | ANDA072096 | HUMAN OTC DRUG | ANDA |
PSEUDOEPHEDRINE HYDROCHLORIDE; IBUPROFEN | 21130-423-41 | Safeway Inc. | ANDA074567 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 76413-344-01 | Central Texas Community Health Centers | ANDA074916 | HUMAN OTC DRUG | ANDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 41520-050-60 | American Sales Company | ANDA079113 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 49035-912-12 | Wal-Mart Stores Inc | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 0363-9601-01 | WALGREENS | ANDA091239 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; DIPHENHYDRAMINE CITRATE | 55111-565-92 | Dr. Reddy's Laboratories Limited | ANDA090619 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; ACETAMINOPHEN | 11822-5777-0 | Rite Aid Corporation | ANDA214836 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41163-604-90 | United Natural Foods, Inc. dba UNFI | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 68210-4201-2 | Spirit Pharmaceuticals LLC | ANDA079129 | HUMAN OTC DRUG | ANDA |
IBUPROFEN SODIUM | 0573-0133-91 | Haleon US Holdings LLC | NDA201803 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 16103-396-04 | Pharbest Pharmaceuticals, Inc. | ANDA091239 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50580-409-12 | Johnson & Johnson Consumer Inc. | ANDA078682 | HUMAN OTC DRUG | ANDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 41520-050-48 | American Sales Company | ANDA079113 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 55910-518-15 | DOLGENCORP INC | ANDA078682 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 49483-611-01 | TIME CAP LABORATORIES,INC | ANDA091237 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 62207-357-91 | Granules India Limited | ANDA202312 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 11673-745-30 | TARGET Corporation | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 59779-685-28 | CVS Pharmacy | ANDA074937 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 63868-977-08 | Chain Drug Marketing Association | ANDA079129 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 58602-708-87 | Aurohealth LLC | ANDA208865 | HUMAN OTC DRUG | ANDA |
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