Sulindac 72789-0374
Product NDC
72789-0374- Manufacturer
- Pd-Rx Pharmaceuticals, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 4, 2009
- Listing Expires
- December 31, 2026
- Application
- ANDA072051
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Sulindac | 200 mg/1 |
Drug Class
Nonsteroidal Anti-inflammatory Drug [EPC]Anti-Inflammatory AgentsNon-Steroidal [CS]
Packaging Options(2)
100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01)
500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82)