Lorazepam

Product NDC
76420-874
11-digit product format
764200874
Labeler code
76420
Product ID
76420-874_263734e7-2ecc-2712-e063-6394a90a6124
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lorazepam
Dosage form
TABLET
Route
ORAL
Labeler
Asclemed USA, Inc.
Application
ANDA076045
Marketing category
ANDA
Marketing start
2023-06-25
Substance
LORAZEPAM
Active strength
2 mg/1
Pharmacologic classes
Benzodiazepine [EPC], Benzodiazepines [CS]
DEA schedule
CIV
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
O26FZP769LLORAZEPAM846-49-1LORAZEPAM

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
76420-874-00764200874001000 TABLET in 1 BOTTLE (76420-874-00) 1000 tablet2024-11-06NoNoHistorical
76420-874-0176420087401100 TABLET in 1 BOTTLE (76420-874-01) 100 tablet2024-11-06NoNoHistorical
76420-874-0576420087405500 TABLET in 1 BOTTLE (76420-874-05) 500 tablet2024-11-06NoNoHistorical
76420-874-307642008743030 TABLET in 1 BOTTLE (76420-874-30) 30 tablet2024-11-06NoNoHistorical
76420-874-607642008746060 TABLET in 1 BOTTLE (76420-874-60) 60 tablet2024-11-06NoNoHistorical
76420-874-907642008749090 TABLET in 1 BOTTLE (76420-874-90) 90 tablet2024-11-06NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Lorazepam Tablets, USP CIVAsclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM2024-11-05HUMAN PRESCRIPTION DRUG LABEL1