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 |
|---|---|---|---|---|---|
| CAPSAICIN; DICLOFENAC SODIUM | 69837-500-05 | International Brand Management, LLC | ANDA202027 | HUMAN PRESCRIPTION DRUG | ANDA |
| CAPSAICIN; DICLOFENAC SODIUM | 70859-004-01 | Nucare Pharmaceuticals Inc | ANDA074514 | HUMAN PRESCRIPTION DRUG | ANDA |
| CAPSAICIN; DICLOFENAC SODIUM | 69336-202-01 | Sterling-Knight Pharmaceuticals, LLC | ANDA075185 | HUMAN PRESCRIPTION DRUG | ANDA |
| CAPSAICIN; DICLOFENAC SODIUM | 81877-645-12 | FORREAL PHARMACEUTICALS LLC | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
| CAPSAICIN; DICLOFENAC SODIUM | 72275-731-77 | Primary Pharmaceuticals, Inc. | ANDA075185 | HUMAN PRESCRIPTION DRUG | ANDA |
| CAPSAICIN; DICLOFENAC SODIUM | 70981-702-01 | Chadwick Pharmaceuticals, Inc | ANDA204132 | HUMAN PRESCRIPTION DRUG | ANDA |
| CAPSAICIN; MENTHOL; DICLOFENAC SODIUM; METHYL SALICYLATE | 70859-045-01 | Nucare Pharmaceuticals Inc | ANDA202769 | HUMAN PRESCRIPTION DRUG | ANDA |
| CAPSICUM OLEORESIN; DICLOFENAC SODIUM | 59088-801-00 | PureTek Corporation | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
| CAPSICUM OLEORESIN; DICLOFENAC SODIUM | 69329-330-00 | Patchwerx Labs, Inc. | ANDA074514 | HUMAN PRESCRIPTION DRUG | ANDA |
| CAPSICUM OLEORESIN; DICLOFENAC SODIUM; RANITIDINE HYDROCHLORIDE | 69329-310-00 | Patchwerx Labs, Inc. | ANDA074514 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC | 42211-203-43 | Iroko Pharmaceuticals LLC | NDA204592 | HUMAN PRESCRIPTION DRUG | NDA |
| DICLOFENAC | 83136-101-15 | Galloping LLC | ANDA211253 | HUMAN OTC DRUG | ANDA |
| DICLOFENAC | 42211-203-23 | Iroko Pharmaceuticals LLC | NDA204592 | HUMAN PRESCRIPTION DRUG | NDA |
| DICLOFENAC | 42211-203-29 | Iroko Pharmaceuticals LLC | NDA204592 | HUMAN PRESCRIPTION DRUG | NDA |
| DICLOFENAC | 42211-204-29 | Iroko Pharmaceuticals LLC | NDA204592 | HUMAN PRESCRIPTION DRUG | NDA |
| DICLOFENAC | 42211-204-23 | Iroko Pharmaceuticals LLC | NDA204592 | HUMAN PRESCRIPTION DRUG | NDA |
| DICLOFENAC | 42211-204-43 | Iroko Pharmaceuticals LLC | NDA204592 | HUMAN PRESCRIPTION DRUG | NDA |
| DICLOFENAC EPOLAMINE | 59762-0707-2 | Greenstone LLC | NDA021234 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
| DICLOFENAC EPOLAMINE | 71858-0405-1 | IBSA Pharma Inc. | NDA021234 | HUMAN PRESCRIPTION DRUG | NDA |
| DICLOFENAC EPOLAMINE | 21695-707-30 | Rebel Distributors Corp. | NDA021234 | HUMAN PRESCRIPTION DRUG | NDA |
| DICLOFENAC EPOLAMINE | 71858-0405-2 | IBSA Pharma Inc. | NDA021234 | HUMAN PRESCRIPTION DRUG | NDA |
| DICLOFENAC EPOLAMINE | 80425-0364-1 | Advanced Rx Pharmacy of Tennessee, LLC | NDA021234 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
| DICLOFENAC EPOLAMINE | 61919-566-30 | DIRECT RX | NDA021234 | HUMAN PRESCRIPTION DRUG | NDA |
| DICLOFENAC EPOLAMINE | 83008-036-30 | Quality Care Products, LLC | NDA021234 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
| DICLOFENAC EPOLAMINE | 55700-886-30 | Quality Care Products, LLC | NDA021234 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
| DICLOFENAC EPOLAMINE | 71858-0305-1 | IBSA Pharma Inc. | NDA206976 | HUMAN PRESCRIPTION DRUG | NDA |
| DICLOFENAC EPOLAMINE | 0093-3727-50 | Teva Pharmaceuticals USA Inc. | NDA021234 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
| DICLOFENAC EPOLAMINE | 82347-0405-4 | YARAL Pharma Inc. | NDA021234 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
| DICLOFENAC EPOLAMINE | 80425-0317-1 | Advanced Rx Pharmacy of Tennessee, LLC | NDA021234 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
| DICLOFENAC EPOLAMINE | 59762-0707-1 | Greenstone LLC | NDA021234 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
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