Zolpidem Tartrate

Product NDC
80425-0153
11-digit product format
804250153
Labeler code
80425
Product ID
80425-0153_2a99bd40-3c4f-3207-e063-6294a90a4faa
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Zolpidem Tartrate
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Advanced Rx Pharmacy of Tennessee, LLC
Application
ANDA078413
Marketing category
ANDA
Marketing start
2007-05-04
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

Additional Listing Data#

Finished product
Yes
Brand name base
Zolpidem Tartrate
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ZOLPIDEM TARTRATE10 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiWY6W63843K
Rxcui854873

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
75543837-e611-4401-8337-81e7d5cb9b04Product name120231011
f40c5cae-52e4-45d3-95e3-8ba7f79e50e4Product name320201208
70793b8c-c4d9-ddb4-5f8a-4308eb0087a2Product name420171109
3970acdc-9e18-4f3d-165e-245802aafc57Product name220160829
438b1497-0992-6caa-062f-3853a7f9e4b1Product name120140508
813c8976-a1f1-3a35-1a71-1557bfb59446Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80425-0153-1Zolpidem Tartrate30 in 1 BOTTLETABLET, FILM COATED308
80425-0153-2Zolpidem Tartrate60 in 1 BOTTLETABLET, FILM COATED608
80425-0153-3Zolpidem Tartrate90 in 1 BOTTLETABLET, FILM COATED908

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
80425-0153-1EA - Each80425-0153d5a940f6-1873-4a4c-8e22-3a2ece3fa07d12023-04-07
80425-0153-2EA - Each80425-015389556b20-2752-4b44-b4db-92593cb5a9a512023-04-07
80425-0153-3EA - Each80425-0153a5995c5e-094c-4cc1-8865-766e5e2b6de412023-04-07

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80425-0153ZOLPIDEM TARTRATE TABLET, FILM COATED [ADVANCED RX PHARMACY OF TENNESSEE, LLC]8Current NDC, Legacy NDC, 3 package rows20250101_c859c752-8a85-2017-e053-2a95a90a771f.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
854873zolpidem tartrate 10 MG Oral TabletPSNc859c752-8a85-2017-e053-2a95a90a771f8
854873zolpidem tartrate 10 MG Oral TabletSCDc859c752-8a85-2017-e053-2a95a90a771f8

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
80425-0153-18042501530130 TABLET, FILM COATED in 1 BOTTLE (80425-0153-1) 2007-05-040000-00-00NoNoCurrent
80425-0153-28042501530260 TABLET, FILM COATED in 1 BOTTLE (80425-0153-2) 2007-05-040000-00-00NoNoCurrent
80425-0153-38042501530390 TABLET, FILM COATED in 1 BOTTLE (80425-0153-3) 2007-05-040000-00-00NoNoCurrent