Alprazolam

Product NDC
35356-504
11-digit product format
353560504
Labeler code
35356
Product ID
35356-504_ccc4fe5e-998d-433c-892e-bf9eed9ffb7d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
alprazolam
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Application
NDA021434
Marketing category
NDA AUTHORIZED GENERIC
Marketing start
2003-01-17
Marketing end
0000-00-00
Substance
ALPRAZOLAM
Active strength
2 mg/1
Pharmacologic classes
Benzodiazepine [EPC],Benzodiazepines [CS]
DEA schedule
CIV
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
35356-504-60EA - Each35356-504714daa80-9587-4010-911f-cd8c4d98572112012-07-24