Eszopiclone 68788-7667
Product NDC
68788-7667- Manufacturer
- Preferred Pharmaceuticals, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIV
- Marketing Start
- February 28, 2020
- Listing Expires
- December 31, 2027
- Application
- ANDA208451
Active Ingredients
| Ingredient | Strength |
|---|---|
| Eszopiclone | 1 mg/1 |
Packaging Options(8)
100 TABLET, FILM COATED in 1 BOTTLE (68788-7667-0)
10 TABLET, FILM COATED in 1 BOTTLE (68788-7667-1)
20 TABLET, FILM COATED in 1 BOTTLE (68788-7667-2)
30 TABLET, FILM COATED in 1 BOTTLE (68788-7667-3)
15 TABLET, FILM COATED in 1 BOTTLE (68788-7667-5)
60 TABLET, FILM COATED in 1 BOTTLE (68788-7667-6)
7 TABLET, FILM COATED in 1 BOTTLE (68788-7667-7)
90 TABLET, FILM COATED in 1 BOTTLE (68788-7667-9)