Lorazepam

Product NDC
76420-647
11-digit product format
764200647
Labeler code
76420
Product ID
76420-647_0b44d6cf-d204-741a-e063-6294a90a05ff
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lorazepam
Dosage form
TABLET
Route
ORAL
Labeler
Asclemed USA, Inc.
Application
ANDA078203
Marketing category
ANDA
Marketing start
2023-05-16
Substance
LORAZEPAM
Active strength
.5 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
76420-647-0176420064701100 TABLET in 1 BOTTLE (76420-647-01) 100 tablet2023-11-29NoNoHistorical
76420-647-307642006473030 TABLET in 1 BOTTLE (76420-647-30) 30 tablet2023-11-29NoNoHistorical
76420-647-607642006476060 TABLET in 1 BOTTLE (76420-647-60) 60 tablet2023-11-29NoNoHistorical
76420-647-907642006479090 TABLET in 1 BOTTLE (76420-647-90) 90 tablet2023-11-29NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Lorazepam Tablets, USP CIV Rx onlyAsclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM2023-11-29HUMAN PRESCRIPTION DRUG LABEL1