NDC 70518-4693

Allopurinol 300 mg tablet

On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Florida Pharmaceutical Products, LLC.'s NDC 71921-242.

United States: 1India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Forma Life Sciences, IncIrvine, CA, United StatesMakes it Problems found, fixed voluntarilyFeb 23, 2024 · 12 inspections
Indoco Remedies LimitedGoa, IndiaMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyJan 20, 2023 · 3 inspections, 1 with FDA action

Product details

Generic drug
Allopurinol: every company that makes it
Form
tablet, oral
Strength
300 mg
Approval
ANDA ANDA204467
On the market since
Jul 7, 2026
Package NDCs
70518-4693-0
Official label
DailyMed (National Library of Medicine), updated Jul 14, 2026

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