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
- 68071-1887_1d601044-106a-4c49-e063-6294a90a8080
- Product NDC
- 68071-1887
- Form
- TABLET
- Composition / generic term
- zolpidem tartrate
- Labeler
- NuCare Pharmaceuticals, Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20070905
- Source listing expiry
- 20261231
Source-listed ingredients
- ZOLPIDEM TARTRATE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 TABLET in 1 BOTTLE (68071-1887-1) · 68071-1887-1
- 20 TABLET in 1 BOTTLE (68071-1887-2) · 68071-1887-2
- 30 TABLET in 1 BOTTLE (68071-1887-3) · 68071-1887-3
- 14 TABLET in 1 BOTTLE (68071-1887-4) · 68071-1887-4
- 15 TABLET in 1 BOTTLE (68071-1887-5) · 68071-1887-5
- 60 TABLET in 1 BOTTLE (68071-1887-6) · 68071-1887-6
- 28 TABLET in 1 BOTTLE (68071-1887-8) · 68071-1887-8
- 90 TABLET in 1 BOTTLE (68071-1887-9) · 68071-1887-9
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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