Clonazepam

Product NDC
66267-708
11-digit product format
662670708
Labeler code
66267
Product ID
66267-708_9cbce27a-aef6-4828-e053-2a95a90a02e7
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
clonazepam
Dosage form
TABLET
Route
ORAL
Labeler
NuCare Pharmaceuticals, Inc.
Application
ANDA077147
Marketing category
ANDA
Marketing start
2011-06-03
Marketing end
0000-00-00
Substance
CLONAZEPAM
Active strength
1 mg/1
Pharmacologic classes
Benzodiazepine [EPC],Benzodiazepines [CS]
DEA schedule
CIV
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
66267-708-306626707083030 TABLET in 1 BOTTLE (66267-708-30) 30 tablet2017-05-170000-00-00NoNoCurrent
66267-708-456626707084545 TABLET in 1 BOTTLE (66267-708-45) 45 tablet2017-05-170000-00-00NoNoCurrent
66267-708-566626707085656 TABLET in 1 BOTTLE (66267-708-56) 56 tablet2017-05-170000-00-00NoNoCurrent
66267-708-606626707086060 TABLET in 1 BOTTLE (66267-708-60) 60 tablet2017-05-170000-00-00NoNoCurrent
66267-708-906626707089090 TABLET in 1 BOTTLE (66267-708-90) 90 tablet2017-05-170000-00-00NoNoCurrent