NDCFind

Eszopiclone 82804-0159

Product NDC

82804-0159
Manufacturer
Proficient Rx Lp
Dosage Form
Tablet, Film Coated
Route
Oral
Product Type
Human Prescription Drug
DEA Schedule
Schedule CIV
Marketing Start
January 4, 2024
Listing Expires
December 31, 2027
Application
ANDA205504

Active Ingredients

IngredientStrength
Eszopiclone1 mg/1

Packaging Options(3)

30 TABLET, FILM COATED in 1 BOTTLE (82804-159-30)

60 TABLET, FILM COATED in 1 BOTTLE (82804-159-60)

90 TABLET, FILM COATED in 1 BOTTLE (82804-159-90)