Eszopiclone 68462-0383
Product NDC
68462-0383- Manufacturer
- Glenmark Pharmaceuticals Inc. Usa
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIV
- Marketing Start
- April 15, 2014
- Listing Expires
- December 31, 2027
- Application
- ANDA091166
Active Ingredients
| Ingredient | Strength |
|---|---|
| Eszopiclone | 2 mg/1 |
Packaging Options(2)
100 TABLET, FILM COATED in 1 BOTTLE (68462-383-01)
1000 TABLET, FILM COATED in 1 BOTTLE (68462-383-10)