NDC 42385-971 – Hydroxychloroquine Sulfate
Hydroxychloroquine Sulfate 200 mg/1 · Tablet, Film Coated · Oral
Product NDC42385-971
Product details
- Brand name
- Hydroxychloroquine Sulfate
- Generic name
- Hydroxychloroquine Sulfate
- Labeler
- Laurus Labs Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA210959
- Marketed since
- March 6, 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 |
|---|---|---|
| 42385-971-01 | 100 TABLET, FILM COATED in 1 BOTTLE (42385-971-01) | Mar 6, 2023 |
| 42385-971-05 | 500 TABLET, FILM COATED in 1 BOTTLE (42385-971-05) | Mar 6, 2023 |
| 42385-971-11 | 1000 TABLET, FILM COATED in 1 BOTTLE (42385-971-11) | Mar 6, 2023 |
| 42385-971-60 | 60 TABLET, FILM COATED in 1 BOTTLE (42385-971-60) | Mar 6, 2023 |
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