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 | 51655-385-54 | Northwind Pharmaceuticals | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 51655-474-20 | Northwind Pharmaceuticals | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 51655-474-25 | Northwind Pharmaceuticals | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 51655-474-26 | Northwind Pharmaceuticals | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 51655-474-51 | Northwind Pharmaceuticals | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 51655-474-52 | Northwind Pharmaceuticals | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 51655-757-26 | Northwind Pharmaceuticals | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 51655-757-52 | Northwind Pharmaceuticals | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 51655-759-52 | Northwind Pharmaceuticals | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 51655-851-20 | Northwind Pharmaceuticals, LLC | ANDA075682 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 51655-851-51 | Northwind Pharmaceuticals, LLC | ANDA075682 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE | 51660-423-21 | Ohm Laboratories Inc. | ANDA074567 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE | 51660-423-41 | Ohm Laboratories Inc. | ANDA074567 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE | 51660-490-41 | Ohm Laboratories Inc. | ANDA074567 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE | 51660-493-41 | Ohm Laboratories Inc. | ANDA074567 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 51672-1385-8 | Taro Pharmaceuticals U.S.A., Inc. | ANDA209204 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 51672-1385-9 | Taro Pharmaceuticals U.S.A., Inc. | ANDA209204 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 51672-1409-8 | Taro Pharmaceuticals U.S.A., Inc. | ANDA209204 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 51672-1409-9 | Taro Pharmaceuticals U.S.A., Inc. | ANDA209204 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 51672-2130-1 | Taro Pharmaceuticals U.S.A., Inc. | ANDA209207 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 51672-2130-8 | Taro Pharmaceuticals U.S.A., Inc. | ANDA209207 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 51672-2144-1 | Taro Pharmaceuticals U.S.A., Inc. | ANDA209207 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 51672-2144-8 | Taro Pharmaceuticals U.S.A., Inc. | ANDA209207 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 51672-2146-3 | Taro Pharmaceuticals U.S.A., Inc. | ANDA217261 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 51824-064-01 | New World Imports | ANDA079174 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 52124-0009-1 | Genuine First Aid LLC | ANDA075010 | HUMAN OTC DRUG | ANDA |
BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE; ASPIRIN; IBUPROFEN; BENZOCAINE; WATER; ALCOHOL; BENZALKONIUM CHLORIDE; LIDOCAINE; ACETAMINOPHEN | 52124-0111-1 | Genuine First Aid LLC | part333 | HUMAN OTC DRUG | OTC monograph final |
NEOMYCIN SULFATE; ISOPROPYL ALCOHOL; WATER; IBUPROFEN; BENZALKONIUM CHLORIDE; BACITRACIN ZINC; BENZOCAINE; POLYMYXIN B SULFATE; ASPIRIN; ALCOHOL; ACETAMINOPHEN; LIDOCAINE | 52124-0112-1 | Genuine First Aid LLC | part333 | HUMAN OTC DRUG | OTC monograph final |
BENZOCAINE; NEOMYCIN SULFATE; ACETAMINOPHEN; ISOPROPYL ALCOHOL; ALCOHOL; ASPIRIN; BENZALKONIUM CHLORIDE; WATER; POLYMYXIN B SULFATE; LIDOCAINE; IBUPROFEN; BACITRACIN ZINC | 52124-0113-1 | Genuine First Aid LLC | part333 | HUMAN OTC DRUG | OTC monograph final |
LIDOCAINE; BENZALKONIUM CHLORIDE; ASPIRIN; IBUPROFEN; ACETAMINOPHEN; ALCOHOL; BENZOCAINE | 52124-0118-1 | Genuine First Aid LLC | part333 | HUMAN OTC DRUG | OTC monograph final |
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