Hydroxychloroquine 62135-0752
Product NDC
62135-0752- Manufacturer
- Chartwell Rx, Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 6, 2018
- Listing Expires
- December 31, 2026
- Application
- ANDA210543
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydroxychloroquine Sulfate | 200 mg/1 |
Drug Class
Antimalarial [EPC]Antirheumatic Agent [EPC]
Packaging Options(1)
90 TABLET in 1 BOTTLE (62135-752-90)