Clonazepam

Product NDC
63739-263
11-digit product format
637390263
Labeler code
63739
Product ID
63739-263_b3c7f09f-f542-452c-e053-2995a90a7c9d
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
1997-02-12
Marketing end
2020-12-31
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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63739-263-102020-07-22C16284748780-1ab0e2407-315a-f274-e053-dbdaa90a6471e0c27a29-b895-4132-a2c2-8da4c0722d03

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63739-263-10EA - Each63739-263d12abba9-ecfc-4b9e-82f5-ec32eb87f75e12012-07-24