Zolpidem Tartrate 16714-0622
Product NDC
16714-0622- Manufacturer
- Northstar Rx 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 Agonists [MoA]Pyridines [CS]
Packaging Options(3)
100 TABLET, FILM COATED in 1 BOTTLE (16714-622-01)
500 TABLET, FILM COATED in 1 BOTTLE (16714-622-02)
10 BLISTER PACK in 1 CARTON (16714-622-11) / 10 TABLET, FILM COATED in 1 BLISTER PACK (16714-622-10)