Zolpidem Tartrate

Product NDC

35356-845

11-digit product format

353560845

Labeler code

35356

Product ID

35356-845_a0f1b181-4d9a-4983-b3f5-7e8797f3e690

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Zolpidem Tartrate

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA078179

Marketing category

ANDA

Marketing start

2010-10-13

Marketing end

0000-00-00

Substance

ZOLPIDEM TARTRATE

Active strength

6 mg/1

Pharmacologic classes

gamma-Aminobutyric Acid-ergic Agonist [EPC],GABA A Agonists [MoA],Pyridines [CS],Central Nervous System Depression [PE]

DEA schedule

CIV

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record