Diclofenac Sodium
- Product NDC
- 50090-0539
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA074514
- Marketing category
- ANDA
- Substance
- DICLOFENAC SODIUM
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 50090-0539-1 | 14 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-0539-1) | 2014-11-28 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| Diclofenac Sodium Delayed-Release Tablets, USP Rx only Prescribing Information | A-S Medication Solutions | 2026-01-15 | HUMAN PRESCRIPTION DRUG LABEL | 29 |