Hydroxychloroquine Sulfate 82619-0131
Product NDC
82619-0131- Manufacturer
- Creekwood Pharmaceuticals Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 8, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA040150
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydroxychloroquine Sulfate | 200 mg/1 |
Drug Class
Antimalarial [EPC]Antirheumatic Agent [EPC]
Packaging Options(3)
100 TABLET in 1 BOTTLE (82619-131-01)
500 TABLET in 1 BOTTLE (82619-131-02)
1000 TABLET in 1 BOTTLE (82619-131-03)