Clonazepam

Product NDC
71335-2509
11-digit product format
713352509
Labeler code
71335
Product ID
71335-2509_fafdf6e5-7b28-4cff-83ae-0a65450a8554
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Clonazepam
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA075468
Marketing category
ANDA
Marketing start
2022-04-14
Substance
CLONAZEPAM
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

Additional Listing Data#

Finished product
Yes
Brand name base
Clonazepam
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
CLONAZEPAM.5 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii5PE9FDE8GB
Rxcui197527

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71335-2509-17133525090120 TABLET in 1 BOTTLE (71335-2509-1) 20 tablet2024-10-21NoNoHistorical
71335-2509-27133525090230 TABLET in 1 BOTTLE (71335-2509-2) 30 tablet2024-10-21NoNoHistorical
71335-2509-37133525090360 TABLET in 1 BOTTLE (71335-2509-3) 60 tablet2024-10-21NoNoHistorical
71335-2509-47133525090490 TABLET in 1 BOTTLE (71335-2509-4) 90 tablet2024-10-21NoNoHistorical
71335-2509-571335250905120 TABLET in 1 BOTTLE (71335-2509-5) 120 tablet2024-10-21NoNoHistorical
71335-2509-67133525090656 TABLET in 1 BOTTLE (71335-2509-6) 56 tablet2024-10-21NoNoHistorical
71335-2509-77133525090728 TABLET in 1 BOTTLE (71335-2509-7) 28 tablet2024-10-21NoNoHistorical
71335-2509-871335250908100 TABLET in 1 BOTTLE (71335-2509-8) 100 tablet2024-10-21NoNoHistorical
71335-2509-97133525090945 TABLET in 1 BOTTLE (71335-2509-9) 45 tablet2024-10-21NoNoHistorical