Lorazepam

Product NDC
63739-804
11-digit product format
637390804
Labeler code
63739
Product ID
63739-804_789d9580-a3e6-495e-bb20-fa3bfc0503cb
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lorazepam
Dosage form
TABLET
Route
ORAL
Labeler
McKesson Corporation dba SKY Packaging
Application
ANDA078203
Marketing category
ANDA
Marketing start
2007-10-01
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#