NDC 80425-0513 – Zolpidem Tartrate

Zolpidem Tartrate 5 mg/1 · Tablet, Coated · Oral

Human Prescription Drug DEA schedule CIV

Product NDC80425-0513

Product details

Brand name
Zolpidem Tartrate
Generic name
Zolpidem Tartrate
Labeler
Advanced Rx of Tennessee, LLC
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA077322
Marketed since
April 15, 2025
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
80425-0513-130 TABLET, COATED in 1 BOTTLE (80425-0513-1)Apr 15, 2025
80425-0513-260 TABLET, COATED in 1 BOTTLE (80425-0513-2)Apr 15, 2025
80425-0513-390 TABLET, COATED in 1 BOTTLE (80425-0513-3)Apr 15, 2025

Other zolpidem tartrate products