Clonazepam

Product NDC
68788-7181
11-digit product format
687887181
Labeler code
68788
Product ID
68788-7181_2a9e73d5-3777-45cb-996c-a3de7ccaadd6
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
clonazepam
Dosage form
TABLET
Route
ORAL
Labeler
Preferred Pharmaceuticals Inc.
Application
ANDA077147
Marketing category
ANDA
Marketing start
2018-07-16
Marketing end
0000-00-00
Substance
CLONAZEPAM
Active strength
2 mg/1
Pharmacologic classes
Benzodiazepine [EPC], Benzodiazepines [CS]
DEA schedule
CIV
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68788-7181-26878871810220 TABLET in 1 BOTTLE, PLASTIC (68788-7181-2) 20 tablet2018-07-160000-00-00NoNoCurrent
68788-7181-36878871810330 TABLET in 1 BOTTLE, PLASTIC (68788-7181-3) 30 tablet2018-07-160000-00-00NoNoCurrent
68788-7181-66878871810660 TABLET in 1 BOTTLE, PLASTIC (68788-7181-6) 60 tablet2018-07-160000-00-00NoNoCurrent
68788-7181-96878871810990 TABLET in 1 BOTTLE, PLASTIC (68788-7181-9) 90 tablet2018-07-160000-00-00NoNoCurrent