NDC 57664-761 – Hydroxychloroquine sulfate
Hydroxychloroquine Sulfate 200 mg/1 · Tablet · Oral
Product NDC57664-761
Product details
- Brand name
- Hydroxychloroquine sulfate
- Generic name
- Hydroxychloroquine sulfate
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA201691
- Marketed since
- June 18, 2018
- 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 57664-761-13 | 500 TABLET in 1 BOTTLE (57664-761-13) | Jun 18, 2018 |
| 57664-761-88 | 100 TABLET in 1 BOTTLE (57664-761-88) | Jun 18, 2018 |
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