Diclofenac Sodium
- Product NDC
- 67296-1225
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA074514
- Marketing category
- ANDA
- Substance
- DICLOFENAC SODIUM
- Current FDA listing
- Historical FDA.report record
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 67296-1225-1 | 21 TABLET, DELAYED RELEASE in 1 BOTTLE (67296-1225-1) | 1996-03-26 | 0000-00-00 | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| 4f2e74ef-9236-2dcb-e054-00144ff8d46c | RedPharm Drug, Inc. | 2022-01-20 | HUMAN PRESCRIPTION DRUG LABEL | 5 |