Hydroxychloroquine Sulfate 16714-0110
Product NDC
16714-0110- Manufacturer
- Northstar Rx Llc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 1, 2019
- 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(2)
100 TABLET, FILM COATED in 1 BOTTLE (16714-110-01)
500 TABLET, FILM COATED in 1 BOTTLE (16714-110-02)