Clonazepam

Product NDC
71335-1856
11-digit product format
713351856
Labeler code
71335
Product ID
71335-1856_722ab62e-0e17-46bb-b170-ac5614ba7fac
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
clonazepam
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA077856
Marketing category
ANDA
Marketing start
2018-02-15
Substance
CLONAZEPAM
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
5PE9FDE8GBCLONAZEPAM1622-61-3CLONAZEPAM

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71335-1856-17133518560130 TABLET in 1 BOTTLE, PLASTIC (71335-1856-1) 30 tablet2021-12-21NoNoHistorical
71335-1856-27133518560260 TABLET in 1 BOTTLE, PLASTIC (71335-1856-2) 60 tablet2021-12-21NoNoHistorical
71335-1856-37133518560390 TABLET in 1 BOTTLE, PLASTIC (71335-1856-3) 90 tablet2021-12-21NoNoHistorical
71335-1856-471335185604120 TABLET in 1 BOTTLE, PLASTIC (71335-1856-4) 120 tablet2021-12-21NoNoHistorical
71335-1856-57133518560510 TABLET in 1 BOTTLE, PLASTIC (71335-1856-5) 10 tablet2021-12-21NoNoHistorical
71335-1856-671335185606180 TABLET in 1 BOTTLE, PLASTIC (71335-1856-6) 180 tablet2021-12-21NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
CLONAZEPAM TABLETS, USP 0.5 mg, 1 mg and 2 mg CIV Rx onlyBryant Ranch Prepack2023-10-26HUMAN PRESCRIPTION DRUG LABEL101