NDC 80425-0066

Lunesta

Eszopiclone 3mg

Lunesta is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Advanced Rx Pharmacy Of Tennessee, Llc. The primary component is Eszopiclone.

• Product ID: 80425-0066_b2126e28-ba89-15cc-e053-2a95a90a5539
• NDC: 80425-0066
• Product Type: Human Prescription Drug
• Proprietary Name: Lunesta
• Generic Name: Eszopiclone 3mg
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2016-09-15
• Marketing Category: ANDA / ANDA
• Application Number: ANDA208451
• Labeler Name: Advanced Rx Pharmacy of Tennessee, LLC
• Substance Name: ESZOPICLONE
• Active Ingredient Strength: 3 mg/1
• DEA Schedule: CIV
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 80425-0066-1

30 TABLET, FILM COATED in 1 BOTTLE (80425-0066-1)

• Marketing Start Date: 2016-09-15
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

NDC Crossover Matching brand name "Lunesta" or generic name "Eszopiclone 3mg"

NDC	Brand Name	Generic Name
21695-225	Lunesta	eszopiclone
21695-226	Lunesta	eszopiclone
50436-0193	Lunesta	ESZOPICLONE
52959-852	Lunesta	ESZOPICLONE
52959-919	Lunesta	ESZOPICLONE
55289-014	Lunesta	ESZOPICLONE
63402-190	Lunesta	ESZOPICLONE
63402-191	Lunesta	ESZOPICLONE
63402-193	Lunesta	ESZOPICLONE
63629-3142	Lunesta	ESZOPICLONE
68258-7048	Lunesta	ESZOPICLONE
68258-7049	Lunesta	ESZOPICLONE
80425-0062	Lunesta	Eszopiclone 2mg
80425-0063	Lunesta	Eszopiclone 2mg
80425-0064	Lunesta	Eszopiclone 2mg
80425-0065	Lunesta	Eszopiclone 3mg
80425-0066	Lunesta	Eszopiclone 3mg
80425-0067	Lunesta	Eszopiclone 3mg
80425-0098	Lunesta	Eszopiclone 1mg
80425-0115	Lunesta	Eszopiclone 3mg
80425-0168	Lunesta	Eszopiclone 1mg