Sulindac 53489-0478
Product NDC
53489-0478- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 4, 2009
- Listing Expires
- December 31, 2026
- Application
- ANDA072050
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Sulindac | 150 mg/1 |
Drug Class
Nonsteroidal Anti-inflammatory Drug [EPC]Anti-Inflammatory AgentsNon-Steroidal [CS]
Packaging Options(6)
100 TABLET in 1 BOTTLE, PLASTIC (53489-478-01)
50 TABLET in 1 BOTTLE, PLASTIC (53489-478-02)
250 TABLET in 1 BOTTLE, PLASTIC (53489-478-03)
500 TABLET in 1 BOTTLE, PLASTIC (53489-478-05)
60 TABLET in 1 BOTTLE, PLASTIC (53489-478-06)
1000 TABLET in 1 BOTTLE, PLASTIC (53489-478-10)