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 |
|---|---|---|---|---|---|
| HYALURONATE SODIUM; NIACINAMIDE; DICLOFENAC SODIUM; CALCIPOTRIENE | 72934-2030-2 | Sincerus Florida, LLC | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
| LEFLUNOMIDE; DICLOFENAC SODIUM | 72835-602-02 | V2 Pharma, LLC | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
| LIDOCAINE HYDROCHLORIDE; DICLOFENAC SODIUM | 53225-1076-1 | Terrain Pharmaceuticals | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
| LIDOCAINE HYDROCHLORIDE; DICLOFENAC SODIUM | 80425-0330-1 | Advanced Rx Pharmacy of Tennessee, LLC | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
| LIDOCAINE; DICLOFENAC SODIUM | 53225-1070-1 | Terrain Pharmaceuticals | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
| LIDOCAINE; MENTHOL, (+)-; DICLOFENAC SODIUM | 73352-565-01 | Trifluent Pharma LLC | M017 | HUMAN OTC DRUG | OTC Monograph Drug |
| MENTHOL; DICLOFENAC SODIUM | 71905-300-01 | Levins Pharmaceuticals, LLC | ANDA203818 | HUMAN PRESCRIPTION DRUG | ANDA |
| MENTHOL; DICLOFENAC SODIUM; CAMPHOR (SYNTHETIC) | 72835-701-02 | V2 Pharma, LLC | ANDA074514 | HUMAN PRESCRIPTION DRUG | ANDA |
| MENTHOL; METHYL SALICYLATE; DICLOFENAC SODIUM | 71437-425-01 | 19 And Pacific, Llc | ANDA208077 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHYL SALICYLATE; DICLOFENAC SODIUM; MENTHOL | 71437-525-01 | 19 And Pacific, Llc | ANDA208077 | HUMAN PRESCRIPTION DRUG | ANDA |
| MISOPROSTOL; DICLOFENAC SODIUM | 71335-1183-3 | Bryant Ranch Prepack | ANDA203995 | HUMAN PRESCRIPTION DRUG | ANDA |
| MISOPROSTOL; DICLOFENAC SODIUM | 42571-134-60 | Micro Labs Limited | ANDA204355 | HUMAN PRESCRIPTION DRUG | ANDA |
| MISOPROSTOL; DICLOFENAC SODIUM | 42291-232-60 | AvKARE | ANDA201089 | HUMAN PRESCRIPTION DRUG | ANDA |
| MISOPROSTOL; DICLOFENAC SODIUM | 10544-955-14 | Blenheim Pharmacal, Inc. | ANDA200540 | HUMAN PRESCRIPTION DRUG | ANDA |
| MISOPROSTOL; DICLOFENAC SODIUM | 42367-110-09 | Eagle Pharmaceuticals, Inc. | ANDA200540 | HUMAN PRESCRIPTION DRUG | ANDA |
| MISOPROSTOL; DICLOFENAC SODIUM | 0025-1411-60 | Pfizer Laboratories Div Pfizer Inc | NDA020607 | HUMAN PRESCRIPTION DRUG | NDA |
| MISOPROSTOL; DICLOFENAC SODIUM | 68001-231-06 | BluePoint Laboratories | ANDA201089 | HUMAN PRESCRIPTION DRUG | ANDA |
| MISOPROSTOL; DICLOFENAC SODIUM | 71335-1183-5 | Bryant Ranch Prepack | ANDA203995 | HUMAN PRESCRIPTION DRUG | ANDA |
| MISOPROSTOL; DICLOFENAC SODIUM | 68001-232-06 | BluePoint Laboratories | ANDA201089 | HUMAN PRESCRIPTION DRUG | ANDA |
| MISOPROSTOL; DICLOFENAC SODIUM | 61919-094-60 | DIRECT RX | ANDA200158 | HUMAN PRESCRIPTION DRUG | ANDA |
| MISOPROSTOL; DICLOFENAC SODIUM | 59762-0028-1 | Greenstone LLC | NDA020607 | HUMAN PRESCRIPTION DRUG | NDA AUTHORIZED GENERIC |
| MISOPROSTOL; DICLOFENAC SODIUM | 71335-1183-1 | Bryant Ranch Prepack | ANDA203995 | HUMAN PRESCRIPTION DRUG | ANDA |
| MISOPROSTOL; DICLOFENAC SODIUM | 75834-264-60 | Nivagen Pharmaceuticals, Inc. | ANDA205143 | HUMAN PRESCRIPTION DRUG | ANDA |
| MISOPROSTOL; DICLOFENAC SODIUM | 42367-110-06 | Eagle Pharmaceuticals, Inc. | ANDA200540 | HUMAN PRESCRIPTION DRUG | ANDA |
| MISOPROSTOL; DICLOFENAC SODIUM | 42291-232-90 | AvKARE | ANDA201089 | HUMAN PRESCRIPTION DRUG | ANDA |
| MISOPROSTOL; DICLOFENAC SODIUM | 68788-8214-3 | Preferred Pharmaceuticals Inc. | ANDA204355 | HUMAN PRESCRIPTION DRUG | ANDA |
| MISOPROSTOL; DICLOFENAC SODIUM | 59762-0028-2 | Greenstone LLC | NDA020607 | HUMAN PRESCRIPTION DRUG | NDA AUTHORIZED GENERIC |
| MISOPROSTOL; DICLOFENAC SODIUM | 0591-0398-60 | Actavis Pharma, Inc. | ANDA201089 | HUMAN PRESCRIPTION DRUG | ANDA |
| MISOPROSTOL; DICLOFENAC SODIUM | 68788-8214-6 | Preferred Pharmaceuticals Inc. | ANDA204355 | HUMAN PRESCRIPTION DRUG | ANDA |
| MISOPROSTOL; DICLOFENAC SODIUM | 0025-1411-90 | Pfizer Laboratories Div Pfizer Inc | NDA020607 | HUMAN PRESCRIPTION DRUG | NDA |
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