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 | 80425-0337-1 | Advanced Rx Pharmacy of Tennessee, LLC | ANDA212506 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 42291-055-12 | AvKARE | ANDA212506 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 83008-019-12 | Quality Care Products, LLC | ANDA212506 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 68788-8541-1 | Preferred Pharmaceuticals Inc. | ANDA213040 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 82804-074-12 | Proficient Rx LP | ANDA213040 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 72189-546-04 | Direct_Rx | ANDA213040 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 13107-269-47 | Aurolife Pharma LLC | ANDA213040 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 59651-353-01 | Aurobindo Pharma Limited | ANDA213875 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 59651-353-08 | Aurobindo Pharma Limited | ANDA213875 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 31722-046-32 | Camber Pharmaceuticals, Inc. | ANDA215375 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 31722-046-31 | Camber Pharmaceuticals, Inc. | ANDA215375 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 70518-3538-0 | REMEDYREPACK INC. | ANDA215585 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 50742-279-01 | Ingenus Pharmaceuticals, LLC | ANDA215585 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 70518-3538-2 | REMEDYREPACK INC. | ANDA215585 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 70518-3538-1 | REMEDYREPACK INC. | ANDA215585 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 68071-2892-3 | NuCare Pharmaceuticals,Inc. | ANDA215585 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 70518-3538-3 | REMEDYREPACK INC. | ANDA215585 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 71335-9720-4 | Bryant Ranch Prepack | ANDA215750 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 71335-9720-2 | Bryant Ranch Prepack | ANDA215750 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 70710-1832-5 | Zydus Pharmaceuticals (USA) Inc. | ANDA215750 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 70710-1832-0 | Zydus Pharmaceuticals (USA) Inc. | ANDA215750 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 60290-057-03 | UMEDICA LABORATORIES PRIVATE LIMITED | ANDA215750 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 71335-9720-1 | Bryant Ranch Prepack | ANDA215750 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 60290-057-02 | UMEDICA LABORATORIES PRIVATE LIMITED | ANDA215750 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 71335-9720-5 | Bryant Ranch Prepack | ANDA215750 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 71335-9720-7 | Bryant Ranch Prepack | ANDA215750 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 50090-6768-0 | A-S Medication Solutions | ANDA215750 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 68071-3451-3 | NuCare Pharmaceuticals,Inc. | ANDA215750 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 60290-057-01 | UMEDICA LABORATORIES PRIVATE LIMITED | ANDA215750 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 71335-9720-8 | Bryant Ranch Prepack | ANDA215750 | HUMAN PRESCRIPTION DRUG | ANDA |
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