NDC 0093-2401 – Hydroxychloroquine Sulfate
Hydroxychloroquine Sulfate 200 mg/1 · Tablet, Film Coated · Oral
Product NDC0093-2401
Product details
- Brand name
- Hydroxychloroquine Sulfate
- Generic name
- Hydroxychloroquine Sulfate
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA040081
- Marketed since
- October 8, 2020
- Marketing end
- November 30, 2026
- Pharmacologic class
- Antimalarial; Antirheumatic Agent
Active ingredients
- Hydroxychloroquine Sulfate 200 mg/1
Uses, dosage, side effects and warnings for Hydroxychloroquine Sulfate →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0093-2401-01 | 100 TABLET, FILM COATED in 1 BOTTLE (0093-2401-01) | Oct 8, 2020 |
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