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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ACETAMINOPHEN; LIDOCAINE; BACITRACIN ZINC; ALCOHOL; POLYMYXIN B SULFATE; IBUPROFEN; NEOMYCIN SULFATE; BENZALKONIUM CHLORIDE; BENZOCAINE | 44224-1999-6 | Tender Corporation DBA Adventure Ready Brands | part348 | HUMAN OTC DRUG | OTC monograph final |
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 |
NEOMYCIN SULFATE; ASPIRIN; BACITRACIN ZINC; BENZOCAINE; ALCOHOL; ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE; BENZALKONIUM CHLORIDE; POLYMYXIN B SULFATE; IBUPROFEN | 44224-3000-1 | Tender Corporation DBA Adventure Ready Brands | part333B | HUMAN OTC DRUG | OTC monograph not final |
DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN; BENZALKONIUM CHLORIDE; NEOMYCIN SULFATE; ASPIRIN; POVIDONE-IODINE; ACETAMINOPHEN; BACITRACIN ZINC; POLYMYXIN B SULFATE | 44224-0118-1 | Tender Corporation DBA Adventure Ready Brands | part333A | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN; NEOMYCIN SULFATE; BACITRACIN ZINC; ALCOHOL; POLYMYXIN B SULFATE; ASPIRIN; BENZALKONIUM CHLORIDE; IBUPROFEN; BENZOCAINE; DIPHENHYDRAMINE HYDROCHLORIDE | 44224-2000-1 | Tender Corporation DBA Adventure Ready Brands | part333B | HUMAN OTC DRUG | OTC monograph not final |
BENZOCAINE; ALCOHOL; POLYMYXIN B SULFATE; IBUPROFEN; ASPIRIN; BACITRACIN ZINC; ACETAMINOPHEN; BENZALKONIUM CHLORIDE; NEOMYCIN SULFATE | 44224-2500-1 | Tender Corporation DBA Adventure Ready Brands | part333B | HUMAN OTC DRUG | OTC monograph not final |
BACITRACIN ZINC; BENZALKONIUM CHLORIDE; BENZOCAINE; IBUPROFEN; ALCOHOL; ACETAMINOPHEN; POLYMYXIN B SULFATE; NEOMYCIN SULFATE | 44224-0699-5 | Tender Corporation DBA Adventure Ready Brands | part348 | HUMAN OTC DRUG | OTC monograph final |
IBUPROFEN; FAMOTIDINE | 0093-8107-98 | Teva Pharmaceuticals USA, Inc. | ANDA211278 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 30142-745-40 | The Kroger Co. | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 30142-743-16 | The Kroger Co. | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 30142-745-30 | The Kroger Co. | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 30142-745-80 | The Kroger Co. | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 30142-743-32 | The Kroger Co. | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 30142-745-16 | The Kroger Co. | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 30142-728-80 | The Kroger Co. | ANDA202300 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 30142-745-02 | The Kroger Co. | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 30142-745-20 | The Kroger Co. | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 30142-743-80 | The Kroger Co. | ANDA206568 | HUMAN OTC DRUG | ANDA |
PSEUDOEPHEDRINE HYDROCHLORIDE; IBUPROFEN | 30142-423-41 | The Kroger Company | ANDA074567 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 73408-509-33 | Thompson Safety | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 73408-809-33 | Thompson Safety | ANDA079174 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 49483-603-05 | TIME CAP LABORATORIES, INC | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 49483-604-05 | TIME CAP LABORATORIES, INC | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 49483-604-01 | TIME CAP LABORATORIES, INC | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 49483-603-03 | TIME CAP LABORATORIES, INC | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 49483-610-44 | TIME CAP LABORATORIES, INC | ANDA079205 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 49483-602-50 | TIME CAP LABORATORIES, INC | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 49483-604-50 | TIME CAP LABORATORIES, INC | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 49483-602-01 | TIME CAP LABORATORIES, INC | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 49483-603-01 | TIME CAP LABORATORIES, INC | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
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