NDC 63402-191

Lunesta

Eszopiclone

Lunesta is a Oral Tablet, Coated in the Human Prescription Drug category. It is labeled and distributed by Sunovion Pharmaceuticals Inc.. The primary component is Eszopiclone.

• Product ID: 63402-191_1b51e0e1-b4a8-43e9-844c-8cd0ee7e784a
• NDC: 63402-191
• Product Type: Human Prescription Drug
• Proprietary Name: Lunesta
• Generic Name: Eszopiclone
• Dosage Form: Tablet, Coated
• Route of Administration: ORAL
• Marketing Start Date: 2005-04-04
• Marketing Category: NDA / NDA
• Application Number: NDA021476
• Labeler Name: Sunovion Pharmaceuticals Inc.
• Substance Name: ESZOPICLONE
• Active Ingredient Strength: 2 mg/1
• DEA Schedule: CIV
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 63402-191-03

30 TABLET, COATED in 1 BOTTLE (63402-191-03)

• Marketing Start Date: 2018-11-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 63402-191-03 [63402019103]

Lunesta TABLET, COATED

• Marketing Category: NDA
• Application Number: NDA021476
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2018-11-01

NDC 63402-191-09 [63402019109]

Lunesta TABLET, COATED

• Marketing Category: NDA
• Application Number: NDA021476
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2005-04-04
• Marketing End Date: 2009-12-19

NDC 63402-191-30 [63402019130]

Lunesta TABLET, COATED

• Marketing Category: NDA
• Application Number: NDA021476
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2009-01-29
• Marketing End Date: 2015-05-31

NDC 63402-191-01 [63402019101]

Lunesta TABLET, COATED

• Marketing Category: NDA
• Application Number: NDA021476
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2009-12-19

NDC 63402-191-10 [63402019110]

Lunesta TABLET, COATED

• Marketing Category: NDA
• Application Number: NDA021476
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2005-04-04

Drug Details

Active Ingredients

Ingredient	Strength
ESZOPICLONE	2 mg/1

OpenFDA Data

• SPL SET ID: fd047b2b-05a6-4d99-95cb-955f14bf329f
• Manufacturer:
  • Sunovion Pharmaceuticals Inc.
• UNII:
  • UZX80K71OE
• RxNorm Concept Unique ID - RxCUI:
  • 485440
  • 485442
  • 540409
  • 485465
  • 540411
  • 540407
• UPC Code:
  • 0363402193030
  • 0363402191036
  • 0363402190305

Medicade Reported Pricing

63402019110 LUNESTA 2 MG TABLET

Pricing Unit: EA | Drug Type:

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

NDC	Brand Name	Generic Name
21695-225	Lunesta	eszopiclone
21695-226	Lunesta	eszopiclone
68258-7048	Lunesta	Lunesta
68258-7049	Lunesta	Lunesta
50436-0193	Lunesta	Lunesta
52959-919	Lunesta	Lunesta
52959-852	Lunesta	Lunesta
55289-014	Lunesta	Lunesta
63402-190	Lunesta	Lunesta
63629-3142	Lunesta	Lunesta
63402-191	Lunesta	Lunesta
63402-193	Lunesta	Lunesta
80425-0115	Lunesta	Lunesta
80425-0064	Lunesta	Lunesta
80425-0062	Lunesta	Lunesta
80425-0098	Lunesta	Lunesta
80425-0066	Lunesta	Lunesta
80425-0067	Lunesta	Lunesta
80425-0065	Lunesta	Lunesta
80425-0063	Lunesta	Lunesta
0054-0290	eszopiclone	eszopiclone
0054-0291	eszopiclone	eszopiclone
0054-0292	eszopiclone	eszopiclone
0093-5537	Eszopiclone	Eszopiclone
0093-5538	Eszopiclone	Eszopiclone
0093-5539	Eszopiclone	Eszopiclone
0378-5270	Eszopiclone	eszopiclone
0378-5271	Eszopiclone	eszopiclone
0378-5272	Eszopiclone	eszopiclone
33342-299	Eszopiclone	Eszopiclone
33342-300	Eszopiclone	Eszopiclone
33342-301	Eszopiclone	Eszopiclone