Clonazepam

Product NDC
63739-264
11-digit product format
637390264
Labeler code
63739
Product ID
63739-264_15dc492e-7b3a-4c94-904a-2fe6eea42cab
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Clonazepam
Dosage form
TABLET
Route
ORAL
Labeler
McKesson Corporation dba SKY Packaging
Application
ANDA074869
Marketing category
ANDA
Marketing start
2007-08-02
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
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63739-264-102020-07-22C16284748780-1ab0e2407-315a-f274-e053-dbdaa90a6471e0c27a29-b895-4132-a2c2-8da4c0722d03

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63739-264-10EA - Each63739-264b79aa86c-6304-4752-96dd-1c09b374cb3f12012-07-24