Hydroxychloroquine Sulfate 71335-0897
Product NDC
71335-0897- Manufacturer
- Bryant Ranch Prepack
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 3, 2008
- Listing Expires
- December 31, 2026
- Application
- ANDA040657
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydroxychloroquine Sulfate | 200 mg/1 |
Drug Class
Antimalarial [EPC]Antirheumatic Agent [EPC]
Packaging Options(9)
100 TABLET, FILM COATED in 1 BOTTLE (71335-0897-1)
30 TABLET, FILM COATED in 1 BOTTLE (71335-0897-2)
60 TABLET, FILM COATED in 1 BOTTLE (71335-0897-3)
180 TABLET, FILM COATED in 1 BOTTLE (71335-0897-4)
90 TABLET, FILM COATED in 1 BOTTLE (71335-0897-5)
120 TABLET, FILM COATED in 1 BOTTLE (71335-0897-6)
10 TABLET, FILM COATED in 1 BOTTLE (71335-0897-7)
14 TABLET, FILM COATED in 1 BOTTLE (71335-0897-8)
20 TABLET, FILM COATED in 1 BOTTLE (71335-0897-9)