NDC 80425-0322 – Zolpidem Tartrate

Zolpidem Tartrate 5 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC80425-0322

Product details

Brand name
Zolpidem Tartrate
Generic name
Zolpidem Tartrate
Labeler
Advanced Rx Pharmacy of Tennessee, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077903
Marketed since
September 5, 2007
Listing expires
December 31, 2026
Pharmacologic class
gamma-Aminobutyric Acid A Receptor Positive Modulator

Active ingredients

Uses, dosage, side effects and warnings for zolpidem tartrate →

Package NDC codes (3)

Package NDCDescriptionSince
80425-0322-130 TABLET in 1 BOTTLE (80425-0322-1)Apr 13, 2023
80425-0322-260 TABLET in 1 BOTTLE (80425-0322-2)Apr 13, 2023
80425-0322-390 TABLET in 1 BOTTLE (80425-0322-3)Apr 13, 2023

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