United States · FDA National Drug Code directory

ZOLPIDEM TARTRATE

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
76420-319_327e6538-4b98-1f09-e063-6294a90a2f75
Product NDC
76420-319
Form
TABLET, EXTENDED RELEASE
Composition / generic term
Zolpidem Tartrate
Labeler
Asclemed USA, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20140411
Source listing expiry
20261231

Source-listed ingredients

  • ZOLPIDEM TARTRATE — 12.5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-319-01) · 76420-319-01
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-319-30) · 76420-319-30
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-319-60) · 76420-319-60
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-319-90) · 76420-319-90

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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