Diclofenac Potassium
- Product NDC
- 68071-2625
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- diclofenac potassium
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA075229
- Marketing category
- ANDA
- Substance
- DICLOFENAC POTASSIUM
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 68071-2625-3 | 30 TABLET, COATED in 1 BOTTLE (68071-2625-3) | 2022-01-21 | | No | Historical |
| 68071-2625-6 | 60 TABLET, COATED in 1 BOTTLE (68071-2625-6) | 2025-01-14 | | No | Historical |
| 68071-2625-9 | 9 TABLET, COATED in 1 BOTTLE (68071-2625-9) | 2022-01-21 | | No | Historical |