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 | 59556-811-25 | Strides Pharma Inc | ANDA206989 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 67091-348-10 | Winco Foods, LLC | ANDA079174 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 71335-2068-2 | Bryant Ranch Prepack | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 58602-858-12 | Aurohealth LLC | ANDA215777 | HUMAN OTC DRUG | ANDA |
PSEUDOEPHEDRINE HYDROCHLORIDE; IBUPROFEN | 0363-0423-41 | WALGREEN COMPANY | ANDA074567 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 55910-074-78 | Dolgencorp, LLC | ANDA077349 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 62207-395-47 | Granules India Limited | ANDA079174 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 49483-133-80 | TIME CAP LABORATORIES, INC. | ANDA079205 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 72476-745-18 | Care One (Retail Business Services, LLC.) | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 62207-366-43 | Granules India Limited | ANDA079174 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 58602-713-36 | Aurohealth LLC | ANDA208865 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 0363-0806-34 | Walgreen Company | ANDA074937 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 21130-396-05 | BETTER LIVING BRANDS LLC. | ANDA079174 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 65162-770-02 | Amneal Pharmaceuticals LLC | ANDA202300 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 69230-308-11 | Camber Consumer Care Inc | ANDA210602 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 51655-757-26 | Northwind Pharmaceuticals | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 11822-0131-2 | Rite Aid Corporation | ANDA203599 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 25000-136-71 | MARKSANS PHARMA LIMITED | ANDA091237 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 0573-0149-91 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 68094-494-58 | Precision Dose Inc. | ANDA074937 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 0573-0151-20 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN SODIUM | 0573-0133-01 | Haleon US Holdings LLC | NDA201803 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 58602-867-92 | Aurohealth LLC | ANDA216204 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 49314-0993-3 | Unishield | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50844-393-14 | L.N.K. International, Inc. | ANDA075139 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41163-312-02 | United Natural Foods, Inc. dba UNFI | ANDA202312 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 37808-057-05 | H E B | ANDA075217 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 67060-001-68 | ADVANCED FIRST AID, INC. | ANDA079174 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 71205-357-30 | Proficient Rx LP | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; ACETAMINOPHEN | 70000-0622-1 | LEADER/ Cardinal Health 110, Inc. | ANDA216592 | HUMAN OTC DRUG | ANDA |
-