Eszopiclone 47335-0586
Product NDC
47335-0586- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- 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, 2026
- Application
- ANDA091103
Active Ingredients
| Ingredient | Strength |
|---|---|
| Eszopiclone | 1 mg/1 |
Packaging Options(4)
100 TABLET, FILM COATED in 1 BOTTLE (47335-586-08)
1000 TABLET, FILM COATED in 1 BOTTLE (47335-586-18)
30 TABLET, FILM COATED in 1 BOTTLE (47335-586-83)
100 TABLET, FILM COATED in 1 BOTTLE (47335-586-88)