FDA Application
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NDC Search Results on Active Ingredient: Diclofenac
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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DICLOFENAC SODIUM | 65162-911-74 | Amneal Pharmaceuticals LLC | ANDA206116 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 68788-7270-1 | Preferred Pharmaceuticals Inc. | ANDA206116 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 70518-0871-0 | REMEDYREPACK INC. | ANDA206116 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 53149-4902-1 | All Pharma, LLC | ANDA206116 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 70518-3464-0 | REMEDYREPACK INC. | ANDA206298 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 68788-8236-1 | Preferred Pharmaceuticals Inc. | ANDA206298 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 72189-040-01 | Direct_Rx | ANDA206298 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 55700-980-00 | Quality Care Products, LLC | ANDA206298 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 71085-003-00 | IPG PHARMACEUTICALS, INC. | ANDA206298 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 50436-0356-1 | UNIT DOSE SERVICES. | ANDA206298 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 51672-1363-7 | Taro Pharmaceuticals U.S.A., Inc. | ANDA206298 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 71205-538-00 | Proficient Rx LP | ANDA206298 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 45865-237-01 | Medsource Pharmaceuticals | ANDA206298 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 76420-275-01 | Asclemed USA, Inc. | ANDA206298 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 45861-063-01 | Pharmaceutica North America, Inc | ANDA206298 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 80425-0235-1 | Advanced Rx Pharmacy of Tennessee, LLC | ANDA206298 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 51672-1363-3 | Taro Pharmaceuticals U.S.A., Inc. | ANDA206298 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 72578-092-01 | Viona Pharmaceuticals Inc | ANDA206411 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 70771-1415-9 | Zydus Lifesciences Limited | ANDA206411 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 71205-752-00 | Proficient Rx LP | ANDA206493 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 76420-261-01 | Asclemed USA, Inc. | ANDA206493 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 0472-1783-10 | Actavis Pharma, Inc. | ANDA206493 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 50436-0357-1 | UNIT DOSE SERVICES. | ANDA206493 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 45865-983-01 | medsource pharmaceuticals | ANDA206715 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 60505-0406-3 | Apotex Corp. | ANDA207714 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 68180-537-01 | Lupin Pharmaceuticals, Inc. | ANDA208021 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 69842-974-17 | CVS Pharmacy | ANDA208077 | HUMAN OTC DRUG | ANDA |
DICLOFENAC SODIUM | 41250-973-17 | MEIJER, INC. | ANDA208077 | HUMAN OTC DRUG | ANDA |
DICLOFENAC SODIUM | 50436-0833-1 | Unit Dose Services | ANDA208077 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 59726-012-53 | P & L Development, LLC | ANDA208077 | HUMAN OTC DRUG | ANDA |
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