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
- 50090-1022_12eb3f4b-6526-4541-a9f3-02be3344a381
- Product NDC
- 50090-1022
- Form
- TABLET
- Composition / generic term
- zolpidem tartrate
- Labeler
- A-S Medication Solutions
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20070905
- Source listing expiry
- 20271231
Source-listed ingredients
- ZOLPIDEM TARTRATE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 20 TABLET in 1 BOTTLE (50090-1022-0) · 50090-1022-0
- 30 TABLET in 1 BOTTLE (50090-1022-1) · 50090-1022-1
- 3 TABLET in 1 BOTTLE (50090-1022-3) · 50090-1022-3
- 60 TABLET in 1 BOTTLE (50090-1022-4) · 50090-1022-4
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 →