Zolpidem Tartrate 16714-0621
Product NDC
16714-0621- 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 | 5 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 (16714-621-01)
500 TABLET, FILM COATED in 1 BOTTLE (16714-621-02)
10 BLISTER PACK in 1 CARTON (16714-621-11) / 10 TABLET, FILM COATED in 1 BLISTER PACK (16714-621-10)