NDC 71610-839 – Zolpidem Tartrate

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

Human Prescription Drug DEA schedule CIV

Product NDC71610-839

Product details

Brand name
Zolpidem Tartrate
Generic name
Zolpidem Tartrate
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA078970
Marketed since
April 11, 2014
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 (4)

Package NDCDescriptionSince
71610-839-3030 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-839-30)Jun 4, 2024
71610-839-5360 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-839-53)Jun 4, 2024
71610-839-6090 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-839-60)Jun 4, 2024
71610-839-80180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-839-80)Jun 4, 2024

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