NDC 69097-994

Diltiazem Hydrochloride 240 mg tablet, extended release

On the label: Cipla USA., Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
ScieGen Pharmaceuticals, INC.Hauppauge, NY, United StatesMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyMay 15, 2026 · 15 inspections, 1 with FDA action

Product details

Generic drug
Diltiazem: every company that makes it
Form
tablet, extended release, oral
Strength
240 mg
Approval
ANDA ANDA216327
On the market since
Jun 12, 2023
Package NDCs
69097-994-02 69097-994-05
Official label
DailyMed (National Library of Medicine), updated Aug 1, 2025

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