NDC 68382-096 – Hydroxychloroquine sulfate
Hydroxychloroquine Sulfate 200 mg/1 · Tablet, Film Coated · Oral
Product NDC68382-096
Product details
- Brand name
- Hydroxychloroquine sulfate
- Generic name
- Hydroxychloroquine sulfate
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA040657
- Marketed since
- January 3, 2008
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 68382-096-01 | 100 TABLET, FILM COATED in 1 BOTTLE (68382-096-01) | Jan 3, 2008 |
| 68382-096-05 | 500 TABLET, FILM COATED in 1 BOTTLE (68382-096-05) | Jan 3, 2008 |
| 68382-096-77 | 100 BLISTER PACK in 1 CARTON (68382-096-77) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68382-096-30) | Jan 3, 2008 |
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