Diazepam

Product NDC
71335-2239
11-digit product format
713352239
Labeler code
71335
Product ID
71335-2239_a4623d8d-0257-43db-bd8a-be652068231a
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
diazepam
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA070325
Marketing category
ANDA
Marketing start
1985-09-04
Substance
DIAZEPAM
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
Q3JTX2Q7TUDIAZEPAM439-14-5DIAZEPAM

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71335-2239-071335223900120 TABLET in 1 BOTTLE, PLASTIC (71335-2239-0) 120 tablet2023-09-22NoNoHistorical
71335-2239-17133522390112 TABLET in 1 BOTTLE, PLASTIC (71335-2239-1) 12 tablet2023-09-22NoNoHistorical
71335-2239-27133522390215 TABLET in 1 BOTTLE, PLASTIC (71335-2239-2) 15 tablet2023-09-22NoNoHistorical
71335-2239-37133522390320 TABLET in 1 BOTTLE, PLASTIC (71335-2239-3) 20 tablet2023-09-22NoNoHistorical
71335-2239-47133522390430 TABLET in 1 BOTTLE, PLASTIC (71335-2239-4) 30 tablet2023-09-22NoNoHistorical
71335-2239-57133522390560 TABLET in 1 BOTTLE, PLASTIC (71335-2239-5) 60 tablet2023-09-22NoNoHistorical
71335-2239-67133522390690 TABLET in 1 BOTTLE, PLASTIC (71335-2239-6) 90 tablet2023-09-22NoNoHistorical
71335-2239-77133522390710 TABLET in 1 BOTTLE, PLASTIC (71335-2239-7) 10 tablet2023-09-22NoNoHistorical
71335-2239-8713352239082 TABLET in 1 BOTTLE, PLASTIC (71335-2239-8) 2 tablet2023-09-22NoNoHistorical
71335-2239-9713352239091 TABLET in 1 BOTTLE, PLASTIC (71335-2239-9) 1 tablet2023-09-22NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Diazepam Tablets, USP 2 mg, 5 mg and 10 mg Rx onlyBryant Ranch Prepack2024-08-23HUMAN PRESCRIPTION DRUG LABEL102