Zolpidem Tartrate 72789-0323
Product NDC
72789-0323- Manufacturer
- Pd-Rx Pharmaceuticals, Inc.
- 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(7)
100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-323-01)
10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-323-10)
14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-323-14)
15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-323-15)
21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-323-21)
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-323-30)
60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-323-60)