Clonazepam

Product NDC
51079-882
11-digit product format
510790882
Labeler code
51079
Product ID
51079-882_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
2020-02-29
Substance
CLONAZEPAM
Active strength
1 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
51079-882-01EA - Each51079-88291443a06-e283-4603-ab6b-20fee86990e412012-07-24
51079-882-20EA - Each51079-882dd78e314-8617-4b3d-8612-a6095f8bb1e712012-07-24
51079-882-21EA - Each51079-882e0b46643-edf6-47ca-a8dc-5e1af8bd87a912012-07-24
51079-882-56EA - Each51079-88231a18ab6-5f94-4805-81bc-9507b9c297c912012-07-24