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 | 83008-033-12 | Quality Care Products, LLC | NDA204623 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
DICLOFENAC SODIUM | 71205-821-12 | Proficient Rx LP | NDA204623 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
DICLOFENAC SODIUM | 72189-498-04 | Direct_Rx | NDA204623 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
DICLOFENAC SODIUM | 70518-3866-0 | REMEDYREPACK INC. | NDA204623 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
DICLOFENAC SODIUM | 0574-0167-12 | Padagis US LLC | NDA204623 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
DICLOFENAC SODIUM | 76420-578-01 | Asclemed USA, Inc. | NDA204623 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
DICLOFENAC SODIUM | 80425-0336-1 | Advanced Rx Pharmacy of Tennessee, LLC | NDA204623 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
DICLOFENAC SODIUM | 75987-040-75 | Horizon Therapeutics USA, Inc. | NDA204623 | HUMAN PRESCRIPTION DRUG | NDA |
DICLOFENAC SODIUM | 63629-9603-1 | Bryant Ranch Prepack | NDA204623 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
DICLOFENAC SODIUM | 75987-040-05 | Horizon Therapeutics USA, Inc. | NDA204623 | HUMAN PRESCRIPTION DRUG | NDA |
DICLOFENAC SODIUM | 75987-040-74 | Horizon Therapeutics USA, Inc. | NDA204623 | HUMAN PRESCRIPTION DRUG | NDA |
DICLOFENAC SODIUM | 70748-335-01 | Lupin Pharmaceuticals, Inc. | NDA204623 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
DICLOFENAC EPOLAMINE | 71858-0305-4 | IBSA Pharma Inc. | NDA206976 | HUMAN PRESCRIPTION DRUG | NDA |
DICLOFENAC EPOLAMINE | 71858-0305-2 | IBSA Pharma Inc. | NDA206976 | HUMAN PRESCRIPTION DRUG | NDA |
DICLOFENAC EPOLAMINE | 71858-0305-5 | IBSA Pharma Inc. | NDA206976 | HUMAN PRESCRIPTION DRUG | NDA |
DICLOFENAC EPOLAMINE | 71858-0305-1 | IBSA Pharma Inc. | NDA206976 | HUMAN PRESCRIPTION DRUG | NDA |
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