NDC 80425-0061 – Zolpidem Tartrate

Zolpidem Tartrate 10 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug DEA schedule CIV

Product NDC80425-0061

Product details

Brand name
Zolpidem Tartrate
Generic name
Zolpidem Tartrate
Labeler
Advanced Rx of Tennessee, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078413
Marketed since
May 4, 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
80425-0061-130 TABLET, FILM COATED in 1 BOTTLE (80425-0061-1)May 4, 2007
80425-0061-260 TABLET, FILM COATED in 1 BOTTLE (80425-0061-2)May 4, 2007
80425-0061-390 TABLET, FILM COATED in 1 BOTTLE (80425-0061-3)May 4, 2007

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