Clonazepam

Product NDC
71610-749
11-digit product format
716100749
Labeler code
71610
Product ID
71610-749_0af09c1a-e64b-4d54-9b26-7e7157208463
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Clonazepam
Dosage form
TABLET
Route
ORAL
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Application
ANDA074569
Marketing category
ANDA
Marketing start
1996-09-18
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
71610-749-157161007491515 TABLET in 1 BOTTLE (71610-749-15) 15 tablet2023-11-15NoNoHistorical
71610-749-307161007493030 TABLET in 1 BOTTLE (71610-749-30) 30 tablet2023-11-15NoNoHistorical
71610-749-457161007494545 TABLET in 1 BOTTLE (71610-749-45) 45 tablet2023-11-15NoNoHistorical
71610-749-537161007495360 TABLET in 1 BOTTLE (71610-749-53) 60 tablet2023-11-15NoNoHistorical
71610-749-607161007496090 TABLET in 1 BOTTLE (71610-749-60) 90 tablet2023-11-15NoNoHistorical
71610-749-8071610074980180 TABLET in 1 BOTTLE (71610-749-80) 180 tablet2023-11-15NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Clonazepam Tablets, USP CIV Rx onlyAphena Pharma Solutions - Tennessee, LLC2023-11-15HUMAN PRESCRIPTION DRUG LABEL1