FDA Application
-
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 POTASSIUM | 70518-3538-0 | REMEDYREPACK INC. | ANDA215585 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC POTASSIUM | 70518-3538-1 | REMEDYREPACK INC. | ANDA215585 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC POTASSIUM | 70518-3538-2 | REMEDYREPACK INC. | ANDA215585 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC POTASSIUM | 70518-3538-3 | REMEDYREPACK INC. | ANDA215585 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 70518-3779-0 | REMEDYREPACK INC. | ANDA212351 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 70518-3866-0 | REMEDYREPACK INC. | NDA204623 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
| DICLOFENAC SODIUM | 70518-4044-0 | REMEDYREPACK INC. | ANDA216275 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 70677-0108-1 | Strategic Sourcing Services LLC | ANDA211253 | HUMAN OTC DRUG | ANDA |
| DICLOFENAC SODIUM | 70677-0143-1 | Strategic Sourcing Services, LLC | ANDA210986 | HUMAN OTC DRUG | ANDA |
| DICLOFENAC SODIUM | 70677-1125-1 | Strategic Sourcing Services, LLC | ANDA210986 | HUMAN OTC DRUG | ANDA |
| DICLOFENAC POTASSIUM | 70710-1832-0 | Zydus Pharmaceuticals (USA) Inc. | ANDA215750 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC POTASSIUM | 70710-1832-1 | Zydus Pharmaceuticals (USA) Inc. | ANDA215750 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC POTASSIUM | 70710-1832-5 | Zydus Pharmaceuticals (USA) Inc. | ANDA215750 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 70748-335-01 | Lupin Pharmaceuticals, Inc. | NDA204623 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
| DICLOFENAC SODIUM | 70771-1415-9 | Zydus Lifesciences Limited | ANDA206411 | HUMAN PRESCRIPTION DRUG | ANDA |
| CAPSAICIN; DICLOFENAC SODIUM | 70859-004-01 | Nucare Pharmaceuticals Inc | ANDA074514 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHYL SALICYLATE; CAPSAICIN; MENTHOL; DICLOFENAC SODIUM | 70859-033-01 | NuCare Pharmaceuticals, Inc. | ANDA074514 | HUMAN PRESCRIPTION DRUG | ANDA |
| MENTHOL; METHYL SALICYLATE; CAPSAICIN; DICLOFENAC SODIUM | 70859-034-01 | NuCare Pharmaceuticals,Inc. | ANDA074514 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM; CAPSAICIN; METHYL SALICYLATE; MENTHOL | 70859-045-01 | Nucare Pharmaceuticals Inc | ANDA202769 | HUMAN PRESCRIPTION DRUG | ANDA |
| CAPSAICIN; MENTHOL; DICLOFENAC SODIUM; METHYL SALICYLATE | 70859-046-01 | NuCare Pharmaceuticals,Inc. | ANDA074514 | HUMAN PRESCRIPTION DRUG | ANDA |
| CAPSAICIN; DICLOFENAC SODIUM | 70859-058-01 | NuCare Pharmaceuticals,Inc. | ANDA202769 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 70882-115-30 | Cambridge Therapeutics Technologies, LLC | ANDA074394 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 70882-128-30 | Cambridge Therapeutics Technologies, LLC | ANDA075185 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 70934-122-30 | Denton Pharma, Inc. DBA Northwind Pharmaceuticals | ANDA075185 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 70934-122-90 | Denton Pharma, Inc. DBA Northwind Pharmaceuticals | ANDA075185 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 70934-678-30 | Denton Pharma, Inc. dba Northwind Pharmaceuticals | ANDA075185 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 70934-678-90 | Denton Pharma, Inc. dba Northwind Pharmaceuticals | ANDA075185 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 70934-687-30 | Denton Pharma, Inc. DBA Northwind Pharmaceuticals | ANDA074514 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM; CAPSAICIN | 70981-702-01 | Chadwick Pharmaceuticals, Inc | ANDA204132 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM; CAPSAICIN | 70981-750-01 | Chadwick Pharmaceuticals, Inc | ANDA204132 | HUMAN PRESCRIPTION DRUG | ANDA |
-
