Hydroxychloroquine Sulfate 57664-0761
Product NDC
57664-0761- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 18, 2018
- Listing Expires
- December 31, 2026
- Application
- ANDA201691
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydroxychloroquine Sulfate | 200 mg/1 |
Drug Class
Antimalarial [EPC]Antirheumatic Agent [EPC]
Packaging Options(2)
500 TABLET in 1 BOTTLE (57664-761-13)
100 TABLET in 1 BOTTLE (57664-761-88)