Zolpidem Tartrate

Product NDC

51079-724

11-digit product format

510790724

Labeler code

51079

Product ID

51079-724_7d8f163b-f2d2-42cc-e053-2991aa0aef2f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

zolpidem tartrate

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Mylan Institutional Inc.

Application

ANDA076578

Marketing category

ANDA

Marketing start

2007-05-01

Marketing end

2019-12-31

Substance

ZOLPIDEM TARTRATE

Active strength

5 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

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record