Clonazepam

Product NDC
51079-883
11-digit product format
510790883
Labeler code
51079
Product ID
51079-883_7df4a15f-f1ab-7cb1-e053-2991aa0acde5
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
clonazepam
Dosage form
TABLET
Route
ORAL
Labeler
Mylan Institutional Inc.
Application
ANDA075150
Marketing category
ANDA
Marketing start
1997-07-15
Marketing end
2020-04-30
Substance
CLONAZEPAM
Active strength
2 mg/1
Pharmacologic classes
Benzodiazepine [EPC],Benzodiazepines [CS]
DEA schedule
CIV
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
51079-883-01EA - Each51079-883806696b5-7a0c-498d-8e10-548f4cc6807312012-07-24
51079-883-20EA - Each51079-8838cf65cd7-915a-4f8a-962f-5479cce0af1a12012-07-24