Hydroxychloroquine Sulfate 82009-0045
Product NDC
82009-0045- Manufacturer
- Quallent Pharmaceuticals Health Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 30, 2022
- Listing Expires
- December 31, 2026
- Application
- ANDA040657
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydroxychloroquine Sulfate | 200 mg/1 |
Drug Class
Antimalarial [EPC]Antirheumatic Agent [EPC]
Packaging Options(1)
500 TABLET, FILM COATED in 1 BOTTLE (82009-045-05)