Lorazepam 2.0 mg per 1 mL injection

Where the pills inside were made

This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Hikma Pharmaceuticals USA Inc. names for other drugs.

Repackaging site

• TYA Pharmaceuticals, Location not on file · repackages it and relabels it

Recalls

• Jul 22, 2025 · Class II · Hikma Pharmaceuticals USA Inc.
  Failed Impurities/Degradation Specifications: An out-of-Specification for total related compounds
  Lots: Lot # K24118, exp. date 10/31/2026
• May 11, 2023 · Class II · Hikma Pharmaceuticals USA Inc.
  Failed Impurities/Degradation Specifications: Out-of-specification results for total related compounds observed during retain steting due to the elevated Related Compound-C.
  Lots: Lots: 070086, 070128, Exp. 07/2023
• Jul 11, 2022 · Class II · Hikma Pharmaceuticals USA Inc.
  Failed Impurities/Degradation Specifications: Out-of-specification results observed for total related compounds during testing of retain samples.
  Lots: Lot # 060064, Exp. 06/2023, 070084, Exp. 07/2023, 070126, Exp. 07/2023, 080091, Exp. 08/2023, 080060, Exp. 08/2023
• Jul 11, 2022 · Class II · Hikma Pharmaceuticals USA Inc.
  Failed Impurities/Degradation Specifications: Out-of-specification results observed for total related compounds during testing of retain samples.
  Lots: Lot # 070096, exp. date 07/2023

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug

Lorazepam: every company that makes it

Form

injection

Strength

2.0 mg per 1 mL

Approval

NDA NDA018140

On the market since

Jul 25, 1980

Package NDCs

64725-6044-1

Official label

DailyMed (National Library of Medicine), updated Nov 15, 2011

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