Where it's 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.
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, intramuscular; intravenous
- Strength
- 4.0 mg per 1 mL
- Approval
- NDA NDA018140
- On the market since
- Jul 25, 1980
- Package NDCs
0641-6047-010641-6047-10- Official label
- DailyMed (National Library of Medicine), updated Apr 9, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?