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
- 16714-622_8d310ac3-c04b-4a08-babe-406d574c5ce3
- Product NDC
- 16714-622
- Form
- TABLET, FILM COATED
- Composition / generic term
- Zolpidem Tartrate
- Labeler
- NorthStar Rx LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20070504
- Source listing expiry
- 20261231
Source-listed ingredients
- ZOLPIDEM TARTRATE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (16714-622-01) · 16714-622-01
- 500 TABLET, FILM COATED in 1 BOTTLE (16714-622-02) · 16714-622-02
- 10 BLISTER PACK in 1 CARTON (16714-622-11) / 10 TABLET, FILM COATED in 1 BLISTER PACK (16714-622-10) · 16714-622-11
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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