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
- 72789-323_2c50fde4-3d33-4137-e063-6394a90a73d6
- Product NDC
- 72789-323
- Form
- TABLET, FILM COATED
- Composition / generic term
- Zolpidem Tartrate
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- 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, PLASTIC (72789-323-01) · 72789-323-01
- 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-323-10) · 72789-323-10
- 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-323-14) · 72789-323-14
- 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-323-15) · 72789-323-15
- 21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-323-21) · 72789-323-21
- 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-323-30) · 72789-323-30
- 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-323-60) · 72789-323-60
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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