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
- 43386-761_b4684db4-fae2-5bc4-e053-2995a90a9cd1
- Product NDC
- 43386-761
- Form
- TABLET
- Composition / generic term
- zolpidem tartrate
- Labeler
- Lupin Pharmaceuticals,Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160322
- Source listing expiry
- 20261231
Source-listed ingredients
- ZOLPIDEM TARTRATE — 3.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 POUCH in 1 CARTON (43386-761-30) / 1 BLISTER PACK in 1 POUCH (43386-761-01) / 1 TABLET in 1 BLISTER PACK · 43386-761-30
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 →