Zolpidem Tartrate
- Product NDC
- 71610-913
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Zolpidem Tartrate
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA204170
- Marketing category
- ANDA
- Substance
- ZOLPIDEM TARTRATE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71610-913-30 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-913-30) | 2025-06-05 | | No | Historical |
| 71610-913-53 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-913-53) | 2025-06-05 | | No | Historical |
| 71610-913-60 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-913-60) | 2025-06-05 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Zolpidem Tartrate | Aphena Pharma Solutions - Tennessee, LLC | 2025-06-09 | Human Prescription Drug Label | 1 |