Hydroxychloroquine Sulfate 43598-0721
Product NDC
43598-0721- Manufacturer
- Dr. Reddy's Laboratories Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 1, 2018
- Listing Expires
- December 31, 2026
- Application
- ANDA210441
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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 (43598-721-01)
500 TABLET, FILM COATED in 1 BOTTLE (43598-721-05)