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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POLYMYXIN B SULFATE; BENZOCAINE; BACITRACIN ZINC; ACETAMINOPHEN; ALCOHOL; IBUPROFEN; BENZALKONIUM CHLORIDE; NEOMYCIN SULFATE | 44224-0999-5 | Tender Corporation DBA Adventure Ready Brands | part348 | HUMAN OTC DRUG | OTC monograph final |
IBUPROFEN; DIPHENHYDRAMINE CITRATE | 66715-6433-2 | Lil' Drug Store Products, Inc. | NDA021394 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 47682-608-30 | Unifirst First Aid Corporation | ANDA075010 | HUMAN OTC DRUG | ANDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 41163-050-27 | United Natural Foods, Inc. dba UNFI | ANDA079113 | HUMAN OTC DRUG | ANDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 0573-0164-32 | Haleon US Holdings LLC | NDA021394 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 55910-604-76 | Dolgencorp, LLC | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 30142-604-93 | Kroger Company | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 0573-0169-22 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 10267-3909-2 | Contract Pharmacal Corp. | ANDA071265 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 0573-0169-49 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 50332-0152-4 | HART Health | M | HUMAN OTC DRUG | OTC Monograph Drug |
IBUPROFEN | 56062-647-85 | Publix Super Markets Inc | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 0113-0298-27 | L. Perrigo Company | ANDA203599 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 42961-203-06 | Cintas Corporation | ANDA079174 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50844-392-14 | L.N.K. International, Inc. | ANDA075139 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 57344-185-01 | AAA Pharmaceutical, Inc. | ANDA079205 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 53942-119-24 | DEMOULAS SUPERMARKETS INC. | ANDA210602 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; IBUPROFEN | 0113-5299-23 | L. Perrigo Company | ANDA214836 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 0904-6747-59 | Major Pharmaceuticals | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 0904-7912-51 | Major Pharmaceuticals | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 72865-132-16 | XLCare Pharmaceuticals, Inc | ANDA206999 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 63187-598-60 | Proficient Rx LP | part343 | HUMAN OTC DRUG | OTC monograph not final |
PHENYLEPHRINE HYDROCHLORIDE; IBUPROFEN | 52904-782-25 | Select Corporation | NDA022565 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 66715-9812-3 | Lil' Drug Store Products, Inc. | ANDA077349 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 68998-012-03 | MARC GLASSMAN, INC. | ANDA202312 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 68210-4200-3 | Spirit Pharmaceuticals LLC | ANDA091355 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 0573-0154-17 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 52959-187-02 | H.J. Harkins Company Inc. dba Pharma Pac | part343 | HUMAN OTC DRUG | OTC MONOGRAPH NOT FINAL |
IBUPROFEN | 37808-393-13 | H E B | ANDA075139 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 0363-9612-50 | WALGREENS | ANDA091237 | HUMAN OTC DRUG | ANDA |
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