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 | 0924-0076-00 | Acme United Corporation | ANDA079174 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 11673-745-80 | TARGET Corporation | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 53943-115-01 | Discount Drug Mart | ANDA091237 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE | 52904-787-03 | Select Corporation | part343 | HUMAN OTC DRUG | OTC MONOGRAPH NOT FINAL |
IBUPROFEN | 41520-897-34 | American Sales Company | ANDA074937 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 21695-065-06 | Rebel Distributors Corp. | ANDA071333 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 82179-001-04 | Mollec Inc | ANDA210602 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 41520-745-18 | Care One (American Sales Company) | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 59726-046-16 | P & L Development, LLC | ANDA207753 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 71205-357-60 | Proficient Rx LP | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 11788-005-10 | AiPing Pharmaceutical, Inc. | ANDA207095 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 25000-117-02 | MARKSANS PHARMA LIMITED | ANDA091239 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 45802-897-34 | Padagis Israel Pharmaceuticals Ltd | ANDA074937 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 59779-604-85 | CVS Pharmacy | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50844-392-16 | L.N.K. International, Inc. | ANDA075139 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; DIPHENHYDRAMINE CITRATE | 30142-050-58 | Kroger Company | ANDA079113 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 55910-604-82 | Dolgencorp, LLC | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 11822-8925-9 | RITE AID | ANDA091237 | HUMAN OTC DRUG | ANDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 0573-0164-08 | Haleon US Holdings LLC | NDA021394 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0363-0225-22 | WALGREEN COMPANY | ANDA078682 | HUMAN OTC DRUG | ANDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 0573-0164-30 | Haleon US Holdings LLC | NDA021394 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 67414-240-09 | Jones Healthcare Group - Packaging Services, Inc | ANDA077349 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50844-352-12 | L.N.K. International, Inc. | ANDA075139 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 55301-393-15 | ARMY AND AIR FORCE EXCHANGE SERVICE | ANDA075139 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 59779-291-10 | CVS Pharmacy | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 55319-199-30 | Family Dollar (FAMILY WELLNESS) | ANDA078682 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; IBUPROFEN | 0113-5300-16 | L Perrigo Company | ANDA214836 | HUMAN OTC DRUG | ANDA |
POLYMYXIN B SULFATE; IBUPROFEN; ISOPROPYL ALCOHOL; BACITRACIN ZINC; NEOMYCIN SULFATE; BENZALKONIUM CHLORIDE; ACETAMINOPHEN | 52124-1000-1 | Genuine First Aid LLC | part333E | HUMAN OTC DRUG | OTC monograph not final |
IBUPROFEN | 55910-847-10 | Dolgencorp, Inc. | ANDA079174 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 0573-0169-30 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
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