NDCFind

Eszopiclone 71205-0633

Product NDC

71205-0633
Manufacturer
Proficient Rx Lp
Dosage Form
Tablet, Film Coated
Route
Oropharyngeal
Product Type
Human Prescription Drug
DEA Schedule
Schedule CIV
Marketing Start
April 15, 2014
Listing Expires
December 31, 2026
Application
ANDA091166

Active Ingredients

IngredientStrength
Eszopiclone3 mg/1

Packaging Options(3)

30 TABLET, FILM COATED in 1 BOTTLE (71205-633-30)

60 TABLET, FILM COATED in 1 BOTTLE (71205-633-60)

90 TABLET, FILM COATED in 1 BOTTLE (71205-633-90)