Celecoxib

Product NDC
82804-213
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Celecoxib
Dosage form
CAPSULE
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA210071
Marketing category
ANDA
Substance
CELECOXIB
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
82804-213-1414 CAPSULE in 1 BOTTLE (82804-213-14) 2025-06-26NoHistorical
82804-213-3030 CAPSULE in 1 BOTTLE (82804-213-30) 2025-04-03NoHistorical
82804-213-6060 CAPSULE in 1 BOTTLE (82804-213-60) 2025-04-21NoHistorical
82804-213-9090 CAPSULE in 1 BOTTLE (82804-213-90) 2025-05-02NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
CelecoxibProficient Rx LP2025-06-01HUMAN PRESCRIPTION DRUG LABEL4