NDC 68071-2332 – Hydroxychloroquine sulfate
Hydroxychloroquine Sulfate 200 mg/1 · Tablet, Film Coated · Oral
Product NDC68071-2332
Product details
- Brand name
- Hydroxychloroquine sulfate
- Generic name
- Hydroxychloroquine sulfate
- Labeler
- NuCare Pharmaceuticals,Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA040657
- Marketed since
- October 1, 2019
- Listing expires
- December 31, 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 |
|---|---|---|
| 68071-2332-1 | 100 TABLET, FILM COATED in 1 BOTTLE (68071-2332-1) | Jan 14, 2021 |
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