NDC 71610-913 – Zolpidem Tartrate

Zolpidem Tartrate 6.25 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug DEA schedule CIV

Product NDC71610-913

Product details

Brand name
Zolpidem Tartrate
Generic name
Zolpidem Tartrate
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA204170
Marketed since
May 15, 2017
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
71610-913-3030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-913-30)Jun 5, 2025
71610-913-5360 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-913-53)Jun 5, 2025
71610-913-6090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-913-60)Jun 5, 2025

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