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; PSEUDOEPHEDRINE HYDROCHLORIDE | 70000-0606-1 | Cardinal Health | ANDA209235 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; ACETAMINOPHEN | 70000-0622-1 | LEADER/ Cardinal Health 110, Inc. | ANDA216592 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; ACETAMINOPHEN | 70000-0622-2 | LEADER/ Cardinal Health 110, Inc. | ANDA216592 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 70005-009-02 | We Care Distributor Inc. | part343 | HUMAN OTC DRUG | OTC monograph not final |
IBUPROFEN | 70005-009-25 | We Care Distributor Inc. | part343 | HUMAN OTC DRUG | OTC monograph not final |
IBUPROFEN | 70005-009-50 | We Care Distributor Inc. | part343 | HUMAN OTC DRUG | OTC monograph not final |
IBUPROFEN; ACETAMINOPHEN | 70010-131-26 | Granules Pharmaceuticals Inc. | ANDA216592 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; ACETAMINOPHEN | 70010-131-31 | Granules Pharmaceuticals Inc. | ANDA216592 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; IBUPROFEN | 70038-131-36 | RAONBIO CORP | ANDA216592 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; IBUPROFEN | 70038-131-72 | RAONBIO CORP | ANDA216592 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; IBUPROFEN | 70038-131-81 | RAONBIO CORP | ANDA216592 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 70253-199-20 | OUR FAMILY (Nash Finch Company) | ANDA078682 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 70253-199-40 | OUR FAMILY (Nash Finch Company) | ANDA078682 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 70253-199-80 | OUR FAMILY (Nash Finch Company) | ANDA078682 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 70264-029-01 | R J General Corporation | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
IBUPROFEN | 70436-180-01 | Slate Run Pharmaceuticals, LLC | ANDA215318 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 70436-180-02 | Slate Run Pharmaceuticals, LLC | ANDA215318 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 70436-181-01 | Slate Run Pharmaceuticals, LLC | ANDA215318 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 70436-181-02 | Slate Run Pharmaceuticals, LLC | ANDA215318 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 70436-182-01 | Slate Run Pharmaceuticals, LLC | ANDA215318 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 70436-182-02 | Slate Run Pharmaceuticals, LLC | ANDA215318 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 70518-0005-0 | REMEDYREPACK INC. | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 70518-0005-1 | REMEDYREPACK INC. | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 70518-0005-2 | REMEDYREPACK INC. | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 70518-0005-3 | REMEDYREPACK INC. | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 70518-0005-4 | REMEDYREPACK INC. | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 70518-0005-5 | REMEDYREPACK INC. | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 70518-0005-6 | REMEDYREPACK INC. | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 70518-0151-0 | REMEDYREPACK INC. | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 70518-0151-1 | REMEDYREPACK INC. | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
-