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 | 50335-0020-1 | Henan Dongtai Pharm Co., Ltd. | BULK INGREDIENT | bulk ingredient for animal drug compounding | |
DICLOFENAC SODIUM | 50383-528-01 | Akorn | ANDA209484 | HUMAN OTC DRUG | ANDA |
DICLOFENAC SODIUM | 50436-0002-1 | Unit Dose Services | ANDA203818 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 50436-0355-1 | Unit Dose Services | ANDA208301 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 50436-0356-1 | UNIT DOSE SERVICES. | ANDA206298 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 50436-0357-1 | UNIT DOSE SERVICES. | ANDA206493 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 50436-0676-1 | Unit Dose Services | ANDA076201 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 50436-0676-2 | Unit Dose Services | ANDA076201 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 50436-0833-1 | Unit Dose Services | ANDA208077 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 50436-1003-1 | Unit Dose Services | ANDA075185 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 50436-1003-2 | Unit Dose Services | ANDA075185 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 50436-1022-1 | Unit Dose Services | ANDA075185 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC EPOLAMINE | 50436-1332-1 | Unit Dose Services | NDA021234 | HUMAN PRESCRIPTION DRUG | NDA |
DICLOFENAC EPOLAMINE | 50436-1335-1 | Unit Dose Services | NDA021234 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
DICLOFENAC SODIUM | 50436-2201-1 | Unit Dose Services | ANDA077863 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 50436-2201-2 | Unit Dose Services | ANDA077863 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 50436-2225-1 | Unit Dose Services | ANDA202769 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 50436-3338-1 | Unit Dose Services | ANDA204132 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 50436-3339-1 | UNIT DOSE SERVICES | ANDA203818 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 50436-3340-1 | UNIT DOSE SERVICES | ANDA206116 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 50436-3621-1 | Unit Dose Services | NDA022122 | HUMAN PRESCRIPTION DRUG | NDA |
DICLOFENAC EPOLAMINE | 50436-3727-1 | Unit Dose Services | NDA021234 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
DICLOFENAC SODIUM | 50436-3990-1 | Unit Dose Services | ANDA202027 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 50436-6924-1 | Unit Dose Services | ANDA077863 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 50436-6924-2 | Unit Dose Services | ANDA077863 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 50436-6925-1 | Unit Dose Services | ANDA075910 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 50436-6925-2 | Unit Dose Services | ANDA075910 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 50580-574-01 | Johnson & Johnson Consumer Inc. | ANDA211253 | HUMAN OTC DRUG | ANDA |
DICLOFENAC SODIUM | 50580-574-02 | Johnson & Johnson Consumer Inc. | ANDA211253 | HUMAN OTC DRUG | ANDA |
DICLOFENAC SODIUM | 50742-278-01 | Ingenus Pharmaceuticals, LLC | ANDA216275 | HUMAN PRESCRIPTION DRUG | ANDA |
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