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
- 71335-0154_23c84f99-953a-4085-b1bd-4bb713a6ac79
- Product NDC
- 71335-0154
- Form
- TABLET
- Composition / generic term
- zolpidem tartrate
- Labeler
- Bryant Ranch Prepack
- 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
- 5 TABLET in 1 BOTTLE (71335-0154-0) · 71335-0154-0
- 30 TABLET in 1 BOTTLE (71335-0154-1) · 71335-0154-1
- 60 TABLET in 1 BOTTLE (71335-0154-2) · 71335-0154-2
- 100 TABLET in 1 BOTTLE (71335-0154-3) · 71335-0154-3
- 50 TABLET in 1 BOTTLE (71335-0154-4) · 71335-0154-4
- 90 TABLET in 1 BOTTLE (71335-0154-5) · 71335-0154-5
- 10 TABLET in 1 BOTTLE (71335-0154-6) · 71335-0154-6
- 15 TABLET in 1 BOTTLE (71335-0154-7) · 71335-0154-7
- 28 TABLET in 1 BOTTLE (71335-0154-8) · 71335-0154-8
- 120 TABLET in 1 BOTTLE (71335-0154-9) · 71335-0154-9
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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