Zolpidem Tartrate 80425-0061
Product NDC
80425-0061- Manufacturer
- Advanced Rx Of Tennessee, Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIV
- Marketing Start
- May 4, 2007
- Listing Expires
- December 31, 2026
- Application
- ANDA078413
Active Ingredients
| Ingredient | Strength |
|---|---|
| Zolpidem Tartrate | 10 mg/1 |
Drug Class
Central Nervous System Depression [PE]GABA A Receptor Positive Modulators [MoA]gamma-Aminobutyric Acid A Receptor Positive Modulator [EPC]
Packaging Options(3)
30 TABLET, FILM COATED in 1 BOTTLE (80425-0061-1)
60 TABLET, FILM COATED in 1 BOTTLE (80425-0061-2)
90 TABLET, FILM COATED in 1 BOTTLE (80425-0061-3)