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
- 63187-862_16ffd293-15a1-4014-9b06-6772decd7651
- Product NDC
- 63187-862
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- zolpidem tartrate
- Labeler
- Proficient Rx LP
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start / end (source format)
- 20101206
- Source listing expiry
- 20261231
Source-listed ingredients
- ZOLPIDEM TARTRATE — 12.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 15 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-862-15) · 63187-862-15
- 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-862-30) · 63187-862-30
- 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-862-60) · 63187-862-60
- 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-862-90) · 63187-862-90
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →