NDC 71335-1771 – Hydroxychloroquine Sulfate
Hydroxychloroquine Sulfate 200 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-1771
Product details
- Brand name
- Hydroxychloroquine Sulfate
- Generic name
- Hydroxychloroquine Sulfate
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA040081
- Marketed since
- October 8, 2020
- 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 (9)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1771-1 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-1771-1) | Sep 2, 2021 |
| 71335-1771-2 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1771-2) | Aug 19, 2021 |
| 71335-1771-3 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-1771-3) | Dec 29, 2021 |
| 71335-1771-4 | 180 TABLET, FILM COATED in 1 BOTTLE (71335-1771-4) | Jan 21, 2021 |
| 71335-1771-5 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1771-5) | Dec 29, 2021 |
| 71335-1771-6 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-1771-6) | Dec 29, 2021 |
| 71335-1771-7 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-1771-7) | Aug 16, 2021 |
| 71335-1771-8 | 14 TABLET, FILM COATED in 1 BOTTLE (71335-1771-8) | Dec 29, 2021 |
| 71335-1771-9 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-1771-9) | Aug 18, 2021 |
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