Celecoxib

Product NDC
50090-7072
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Celecoxib
Dosage form
CAPSULE
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA210071
Marketing category
ANDA
Substance
CELECOXIB
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-7072-090 CAPSULE in 1 BOTTLE (50090-7072-0) 2024-01-22NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
CelecoxibA-S Medication Solutions2024-08-21HUMAN PRESCRIPTION DRUG LABEL1