Zolpidem Tartrate

Product NDC
80425-0301
11-digit product format
804250301
Labeler code
80425
Product ID
80425-0301_2a9b9724-025a-e829-e063-6394a90a1c07
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Zolpidem Tartrate
Dosage form
TABLET
Route
ORAL
Labeler
Advanced Rx Pharmacy of Tennessee, LLC
Application
ANDA077903
Marketing category
ANDA
Marketing start
2023-04-07
Substance
ZOLPIDEM TARTRATE
Active strength
10 mg/1
Pharmacologic classes
Central Nervous System Depression [PE], GABA A Receptor Positive Modulators [MoA], gamma-Aminobutyric Acid A Receptor Positive Modulator [EPC]
DEA schedule
CIV
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
WY6W63843KZOLPIDEM TARTRATE99294-93-6ZOLPIDEM TARTRATE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
80425-0301-18042503010130 TABLET in 1 BOTTLE (80425-0301-1) 30 tablet2023-04-07NoNoHistorical
80425-0301-28042503010260 TABLET in 1 BOTTLE (80425-0301-2) 60 tablet2023-04-07NoNoHistorical
80425-0301-38042503010390 TABLET in 1 BOTTLE (80425-0301-3) 90 tablet2023-04-07NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Zolpidem Tartrate TabletsAdvanced Rx Pharmacy of Tennessee, LLC2024-12-31HUMAN PRESCRIPTION DRUG LABEL2