Eszopiclone

Product NDC
82804-076
11-digit product format
828040076
Labeler code
82804
Product ID
82804-076_e32746a8-6440-4b0a-a445-4467cf0329d5
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Eszopiclone
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA091166
Marketing category
ANDA
Marketing start
2014-04-15
Substance
ESZOPICLONE
Active strength
2 mg/1
DEA schedule
CIV
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

openFDA Listing Details

Product ID
82804-076_e32746a8-6440-4b0a-a445-4467cf0329d5
SPL ID
e32746a8-6440-4b0a-a445-4467cf0329d5
Product type
HUMAN PRESCRIPTION DRUG
Finished product
Yes
Brand name base
Eszopiclone
Generic name
Eszopiclone
Dosage form
TABLET, FILM COATED
Route
ORAL
Marketing start
2014-04-15
Marketing category
ANDA
Application number
ANDA091166
DEA schedule
CIV
Listing expiration
2026-12-31

openFDA Active Ingredients

IngredientStrength
ESZOPICLONE2 mg/1

openFDA Harmonized Identifiers

FieldValues
UniiUZX80K71OE
Rxcui485442
Spl Set Ide32746a8-6440-4b0a-a445-4467cf0329d5
Manufacturer NameProficient Rx LP

openFDA Package Details

Package NDCDescriptionMarketing startSample
82804-076-3030 TABLET, FILM COATED in 1 BOTTLE (82804-076-30)2024-02-21No
82804-076-6060 TABLET, FILM COATED in 1 BOTTLE (82804-076-60)2024-02-21No
82804-076-9090 TABLET, FILM COATED in 1 BOTTLE (82804-076-90)2024-02-21No

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
UZX80K71OEESZOPICLONE138729-47-2ESZOPICLONE

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
82804-076-308280400763030 TABLET, FILM COATED in 1 BOTTLE (82804-076-30) 2024-02-21NoNoHistorical
82804-076-608280400766060 TABLET, FILM COATED in 1 BOTTLE (82804-076-60) 2024-02-21NoNoHistorical
82804-076-908280400769090 TABLET, FILM COATED in 1 BOTTLE (82804-076-90) 2024-02-21NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
EszopicloneProficient Rx LP2024-02-01HUMAN PRESCRIPTION DRUG LABEL1