Lorazepam

Product NDC
71610-827
11-digit product format
716100827
Labeler code
71610
Product ID
71610-827_334dd50d-b89b-af1b-e063-6294a90ad9bf
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lorazepam
Dosage form
TABLET
Route
ORAL
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Application
ANDA076045
Marketing category
ANDA
Marketing start
2023-10-26
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
71610-827-107161008271010 TABLET in 1 BOTTLE (71610-827-10) 10 tablet2024-05-02NoNoHistorical
71610-827-157161008271515 TABLET in 1 BOTTLE (71610-827-15) 15 tablet2024-05-08NoNoHistorical
71610-827-207161008272020 TABLET in 1 BOTTLE (71610-827-20) 20 tablet2024-05-08NoNoHistorical
71610-827-287161008272828 TABLET in 1 BOTTLE (71610-827-28) 28 tablet2024-05-02NoNoHistorical
71610-827-307161008273030 TABLET in 1 BOTTLE (71610-827-30) 30 tablet2024-05-02NoNoHistorical
71610-827-457161008274545 TABLET in 1 BOTTLE (71610-827-45) 45 tablet2024-05-02NoNoHistorical
71610-827-537161008275360 TABLET in 1 BOTTLE (71610-827-53) 60 tablet2024-05-02NoNoHistorical
71610-827-607161008276090 TABLET in 1 BOTTLE (71610-827-60) 90 tablet2024-05-02NoNoHistorical
71610-827-7071610082770120 TABLET in 1 BOTTLE (71610-827-70) 120 tablet2024-06-05NoNoHistorical
71610-827-7571610082775150 TABLET in 1 BOTTLE (71610-827-75) 150 tablet2025-04-15NoNoHistorical
71610-827-8071610082780180 TABLET in 1 BOTTLE (71610-827-80) 180 tablet2024-05-02NoNoHistorical
71610-827-9271610082792270 TABLET in 1 BOTTLE (71610-827-92) 270 tablet2024-05-02NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Lorazepam Tablets, USP CIVAphena Pharma Solutions - Tennessee, LLC2025-04-21HUMAN PRESCRIPTION DRUG LABEL4