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 |
|---|---|---|---|---|---|
| DICLOFENAC SODIUM | 68071-3516-1 | NuCare Pharmaceuticals,Inc. | ANDA208301 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 68071-3556-7 | NuCare Pharmaceuticals,Inc. | ANDA076201 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 68071-4117-2 | NuCare Pharmaceuticals,Inc. | ANDA075185 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 68071-4117-3 | NuCare Pharmaceuticals,Inc. | ANDA075185 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 68071-4117-4 | NuCare Pharmaceuticals,Inc. | ANDA075185 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 68071-4117-6 | NuCare Pharmaceuticals,Inc. | ANDA075185 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 68071-4117-9 | NuCare Pharmaceuticals,Inc. | ANDA075185 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 68071-4158-2 | NuCare Pharmaceuticals,Inc. | ANDA075492 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 68071-4231-1 | NuCare Pharmaceuticals,Inc. | ANDA075185 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 68071-4231-3 | NuCare Pharmaceuticals,Inc. | ANDA075185 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 68071-4231-5 | NuCare Pharmaceuticals,Inc. | ANDA075185 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 68071-4231-6 | NuCare Pharmaceuticals,Inc. | ANDA075185 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 68071-4231-9 | NuCare Pharmaceuticals,Inc. | ANDA075185 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 68071-4382-1 | NuCare Pharmaceuticals,Inc. | NDA022122 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
| DICLOFENAC SODIUM | 68071-4859-1 | NuCare Pharmaceuticals,Inc. | ANDA210893 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 68071-4934-4 | NuCare Pharmaceuticals,Inc. | ANDA075185 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC POTASSIUM | 68151-0561-0 | Carilion Materials Management | ANDA075219 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 68151-0849-1 | Carilion Materials Management | ANDA090066 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 68151-2481-0 | Carilion Materials Management | ANDA074376 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 68180-537-01 | Lupin Pharmaceuticals, Inc. | ANDA208021 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 68180-538-01 | Lupin Pharmaceuticals, Inc. | ANDA204132 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 68196-870-03 | Sam's West Inc | ANDA211253 | HUMAN OTC DRUG | ANDA |
| DICLOFENAC SODIUM | 68196-870-05 | Sam's West Inc | ANDA211253 | HUMAN OTC DRUG | ANDA |
| DICLOFENAC SODIUM | 68387-260-20 | Keltman Pharmaceuticals, Inc. | ANDA077863 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 68387-260-30 | Keltman Pharmaceuticals, Inc. | ANDA077863 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 68387-260-60 | Keltman Pharmaceuticals, Inc. | ANDA077863 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 68387-456-01 | Keltman Pharmaceuticals, Inc. | NDA022122 | HUMAN PRESCRIPTION DRUG | NDA |
| DICLOFENAC SODIUM | 68391-205-00 | BJWC | ANDA211253 | HUMAN OTC DRUG | ANDA |
| DICLOFENAC SODIUM | 68462-355-94 | GLENMARK PHARMACEUTICALS INC., USA | ANDA208301 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 68682-103-01 | Oceanside Pharmaceuticals | ANDA075492 | HUMAN PRESCRIPTION DRUG | ANDA |
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