Eszopiclone 68180-0322
Product NDC
68180-0322- Manufacturer
- Lupin Pharmaceuticals, 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
- ANDA091124
Active Ingredients
| Ingredient | Strength |
|---|---|
| Eszopiclone | 1 mg/1 |
Packaging Options(1)
100 TABLET, FILM COATED in 1 BOTTLE (68180-322-01)