Eszopiclone 68788-7029
Product NDC
68788-7029- Manufacturer
- Preferred Pharmaceuticals Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIV
- Marketing Start
- October 12, 2017
- Listing Expires
- December 31, 2027
- Application
- ANDA202929
Active Ingredients
| Ingredient | Strength |
|---|---|
| Eszopiclone | 2 mg/1 |
Packaging Options(5)
10 TABLET, FILM COATED in 1 BOTTLE (68788-7029-1)
20 TABLET, FILM COATED in 1 BOTTLE (68788-7029-2)
30 TABLET, FILM COATED in 1 BOTTLE (68788-7029-3)
60 TABLET, FILM COATED in 1 BOTTLE (68788-7029-6)
90 TABLET, FILM COATED in 1 BOTTLE (68788-7029-9)