NDC 71335-3113

Hydroxychloroquine Sulfate 200 mg tablet

On the label: Bryant Ranch Prepack. It's repackaged: Bryant Ranch Prepack rebottles it from Creekwood Pharmaceuticals LLC's NDC 82619-131.

India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
V-Ensure Pharma Technologies Pvt LimitedRaigad, IndiaMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyMay 17, 2024 · 2 inspections

Repackaging site

Product details

Generic drug
Hydroxychloroquine: every company that makes it
Form
tablet, oral
Strength
200 mg
Approval
ANDA ANDA040150
On the market since
May 8, 2025
Package NDCs
71335-3113-1 71335-3113-2 71335-3113-3 71335-3113-4 71335-3113-5 71335-3113-6 71335-3113-7 71335-3113-8 71335-3113-9
Official label
DailyMed (National Library of Medicine), updated Mar 30, 2026

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