NDC 70752-295

Niacin 500 mg tablet, extended release

On the label: Quagen Pharmaceuticals LLC.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Lannett Company, LLCSeymour, IN, United StatesMakes it and packages it Problems found, fixed voluntarilyOct 21, 2022 · 9 inspections, 1 with FDA action

Product details

Generic drug
Niacin: every company that makes it
Form
tablet, extended release, oral
Strength
500 mg
Approval
ANDA ANDA203899
On the market since
Aug 6, 2026
Package NDCs
70752-295-09
Official label
DailyMed (National Library of Medicine), updated Dec 25, 2025

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