Eszopiclone 61919-0033
Product NDC
61919-0033- Manufacturer
- Direct Rx
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIV
- Marketing Start
- February 13, 2017
- Listing Expires
- December 31, 2027
- Application
- ANDA202929
Active Ingredients
| Ingredient | Strength |
|---|---|
| Eszopiclone | 2 mg/1 |
Packaging Options(3)
10 TABLET, FILM COATED in 1 BOTTLE (61919-033-10)
30 TABLET, FILM COATED in 1 BOTTLE (61919-033-30)
60 TABLET, FILM COATED in 1 BOTTLE (61919-033-60)