SULINDAC
- Product NDC
- 72789-373
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- sulindac
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA072050
- Marketing category
- ANDA
- Substance
- SULINDAC
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 72789-373-01 | 100 TABLET in 1 BOTTLE, PLASTIC (72789-373-01) | 2024-01-19 | | No | Historical |
| 72789-373-82 | 500 TABLET in 1 BOTTLE, PLASTIC (72789-373-82) | 2024-01-25 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| SULINDAC TABLETS USP | PD-Rx Pharmaceuticals, Inc. | 2025-10-23 | HUMAN PRESCRIPTION DRUG LABEL | 22 |
| SULINDAC TABLETS USP | PD-Rx Pharmaceuticals, Inc. | 2025-04-04 | HUMAN PRESCRIPTION DRUG LABEL | 21 |