Zolpidem Tartrate

Product NDC

70518-0161

11-digit product format

705180161

Labeler code

70518

Product ID

70518-0161_812ceae3-80af-73b7-e053-2991aa0ab5bd

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

zolpidem tartrate

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA076578

Marketing category

ANDA

Marketing start

2017-01-23

Marketing end

0000-00-00

Substance

ZOLPIDEM TARTRATE

Active strength

10 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

2020-12-31

Current FDA listing

Historical FDA.report record