NDC 43598-721 – Hydroxychloroquine Sulfate
Hydroxychloroquine Sulfate 200 mg/1 · Tablet, Film Coated · Oral
Product NDC43598-721
Product details
- Brand name
- Hydroxychloroquine Sulfate
- Generic name
- Hydroxychloroquine Sulfate
- Labeler
- Dr. Reddy's Laboratories Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA210441
- Marketed since
- May 1, 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 |
|---|---|---|
| 43598-721-01 | 100 TABLET, FILM COATED in 1 BOTTLE (43598-721-01) | May 1, 2018 |
| 43598-721-05 | 500 TABLET, FILM COATED in 1 BOTTLE (43598-721-05) | May 1, 2018 |
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