Hydroxychloroquine Sulfate 71335-3079
Product NDC
71335-3079- Manufacturer
- Bryant Ranch Prepack
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 3, 2024
- Listing Expires
- December 31, 2027
- Application
- ANDA040766
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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 (71335-3079-1)
30 TABLET, FILM COATED in 1 BOTTLE (71335-3079-2)
60 TABLET, FILM COATED in 1 BOTTLE (71335-3079-3)
180 TABLET, FILM COATED in 1 BOTTLE (71335-3079-4)
90 TABLET, FILM COATED in 1 BOTTLE (71335-3079-5)
120 TABLET, FILM COATED in 1 BOTTLE (71335-3079-6)
10 TABLET, FILM COATED in 1 BOTTLE (71335-3079-7)
14 TABLET, FILM COATED in 1 BOTTLE (71335-3079-8)
20 TABLET, FILM COATED in 1 BOTTLE (71335-3079-9)