Zolpidem Tartrate

Product NDC

50436-3030

11-digit product format

504363030

Labeler code

50436

Product ID

50436-3030_efa32477-9a65-4f9f-bc2d-02c059bb8a4c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

zolpidem tartrate

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Unit Dose Services

Application

ANDA078616

Marketing category

ANDA

Marketing start

2008-11-21

Marketing end

0000-00-00

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

2019-12-31

Current FDA listing

Historical FDA.report record