NDCFind

Eszopiclone 71205-0236

Product NDC

71205-0236
Manufacturer
Proficient Rx Lp
Dosage Form
Tablet, Film Coated
Route
Oral
Product Type
Human Prescription Drug
DEA Schedule
Schedule CIV
Marketing Start
September 15, 2016
Listing Expires
December 31, 2026
Application
ANDA208451

Active Ingredients

IngredientStrength
Eszopiclone3 mg/1

Packaging Options(3)

30 TABLET, FILM COATED in 1 BOTTLE (71205-236-30)

60 TABLET, FILM COATED in 1 BOTTLE (71205-236-60)

90 TABLET, FILM COATED in 1 BOTTLE (71205-236-90)