Diclofenac Sodium
- Product NDC
- 68071-3556
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac Sodium
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA076201
- Marketing category
- ANDA
- Substance
- DICLOFENAC SODIUM
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 68071-3556-7 | 7 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68071-3556-7) | 2023-12-22 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Diclofenac Sodium | NuCare Pharmaceuticals,Inc. | 2025-02-03 | HUMAN PRESCRIPTION DRUG LABEL | 2 |