Diclofenac Potassium
- Product NDC
- 71335-2052
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- diclofenac potassium
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075229
- Marketing category
- ANDA
- Substance
- DICLOFENAC POTASSIUM
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71335-2052-1 | 20 TABLET, COATED in 1 BOTTLE (71335-2052-1) | 20220318 | | No | Historical |
Related DailyMed Labels
| Set ID | Title | Manufacturer | Effective date | Type | Version |
|---|
| 86461915-9bc1-43d4-8d92-6eef3e56bd90 | Diclofenac Potassium Tablets, USP 25 mg and 50 mg | Bryant Ranch Prepack | 2024-01-17 | HUMAN PRESCRIPTION DRUG LABEL | 103 |