Lorazepam

Product NDC
63739-501
11-digit product format
637390501
Labeler code
63739
Product ID
63739-501_4c7f9699-b7de-4fbd-8e94-dfc590847b3f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lorazepam
Dosage form
TABLET
Route
ORAL
Labeler
McKesson Corporation dba SKY Packaging
Application
ANDA072928
Marketing category
ANDA
Marketing start
1991-10-31
Marketing end
0000-00-00
Substance
LORAZEPAM
Active strength
2 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
63739-501-102020-07-22C16284748780-1ab0e2407-3160-f274-e053-dbdaa90a6471f16b9773-aaef-4ae6-a216-66d0df2df167

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63739-501-10EA - Each63739-50164ef4ca3-ec63-4201-914a-e81b6171563612012-07-24