Hydroxychloroquine Sulfate 16571-0112
Product NDC
16571-0112- Manufacturer
- Rising Pharma Holdings, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 29, 2023
- Listing Expires
- December 31, 2026
- Application
- ANDA210959
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydroxychloroquine Sulfate | 200 mg/1 |
Drug Class
Antimalarial [EPC]Antirheumatic Agent [EPC]
Packaging Options(4)
100 TABLET, FILM COATED in 1 BOTTLE (16571-112-01)
60 TABLET, FILM COATED in 1 BOTTLE (16571-112-06)
1000 TABLET, FILM COATED in 1 BOTTLE (16571-112-10)
500 TABLET, FILM COATED in 1 BOTTLE (16571-112-50)