Diclofenac Sodium
- Product NDC
- 50090-1769
- 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
- Historical FDA.report record
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 50090-1769-0 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-1769-0) | 2015-04-07 | 0000-00-00 | No | Current |
| 50090-1769-1 | 20 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-1769-1) | 2015-04-07 | 0000-00-00 | No | Current |
| 50090-1769-2 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-1769-2) | 2015-04-07 | 0000-00-00 | No | Current |
| 50090-1769-3 | 14 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-1769-3) | 2015-04-07 | 0000-00-00 | No | Current |
| 50090-1769-4 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-1769-4) | 2015-04-07 | 0000-00-00 | No | Current |
| 50090-1769-8 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-1769-8) | 2015-07-17 | 0000-00-00 | No | Current |
| 50090-1769-9 | 180 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-1769-9) | 2019-08-05 | 0000-00-00 | No | Current |