NDC 16571-112 – Hydroxychloroquine Sulfate
Hydroxychloroquine Sulfate 200 mg/1 · Tablet, Film Coated · Oral
Product NDC16571-112
Product details
- Brand name
- Hydroxychloroquine Sulfate
- Generic name
- Hydroxychloroquine Sulfate
- Labeler
- Rising Pharma Holdings, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA210959
- Marketed since
- May 29, 2023
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 16571-112-01 | 100 TABLET, FILM COATED in 1 BOTTLE (16571-112-01) | May 29, 2023 |
| 16571-112-06 | 60 TABLET, FILM COATED in 1 BOTTLE (16571-112-06) | May 29, 2023 |
| 16571-112-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (16571-112-10) | May 29, 2023 |
| 16571-112-50 | 500 TABLET, FILM COATED in 1 BOTTLE (16571-112-50) | May 29, 2023 |
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