NDC 71335-3142 – Hydroxychloroquine Sulfate
Hydroxychloroquine Sulfate 200 mg/1 · Tablet · Oral
Product NDC71335-3142
Product details
- Brand name
- Hydroxychloroquine Sulfate
- Generic name
- Hydroxychloroquine sulfate
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA040150
- Marketed since
- May 8, 2025
- Listing expires
- December 31, 2027
- Pharmacologic class
- Antimalarial; Antirheumatic Agent
Active ingredients
- Hydroxychloroquine Sulfate 200 mg/1
Uses, dosage, side effects and warnings for Hydroxychloroquine Sulfate →
Package NDC codes (9)
| Package NDC | Description | Since |
|---|---|---|
| 71335-3142-1 | 100 TABLET in 1 BOTTLE (71335-3142-1) | Jun 8, 2026 |
| 71335-3142-2 | 30 TABLET in 1 BOTTLE (71335-3142-2) | Jun 8, 2026 |
| 71335-3142-3 | 60 TABLET in 1 BOTTLE (71335-3142-3) | Jun 8, 2026 |
| 71335-3142-4 | 180 TABLET in 1 BOTTLE (71335-3142-4) | Jun 8, 2026 |
| 71335-3142-5 | 90 TABLET in 1 BOTTLE (71335-3142-5) | Jun 8, 2026 |
| 71335-3142-6 | 120 TABLET in 1 BOTTLE (71335-3142-6) | Jun 8, 2026 |
| 71335-3142-7 | 10 TABLET in 1 BOTTLE (71335-3142-7) | Jun 8, 2026 |
| 71335-3142-8 | 14 TABLET in 1 BOTTLE (71335-3142-8) | Jun 8, 2026 |
| 71335-3142-9 | 20 TABLET in 1 BOTTLE (71335-3142-9) | Jun 8, 2026 |
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- 71610-701 Hydroxychloroquine Sulfate 200 mg/1 · Tablet · Aphena Pharma Solutions - Tennessee, LLC
- 71335-2814 Hydroxychloroquine Sulfate 200 mg/1 · Tablet · Bryant Ranch Prepack
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