NDC 0121-0770

Lorazepam 2 mg per 1 mL liquid

On the label: Pharmaceutical Associates, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
PAI Holdings, LLC dba Pharmaceutical Associates, Inc. and dba PAI PharmaGreenville, SC, United StatesMakes it No problems foundAug 1, 2025 · 18 inspections, 1 with FDA action

Product details

Generic drug
Lorazepam: every company that makes it
Form
liquid, oral
Strength
2 mg per 1 mL
Approval
ANDA ANDA090260
On the market since
Nov 1, 2010
Package NDCs
0121-0770-01
Official label
DailyMed (National Library of Medicine), updated Oct 30, 2026

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