Chlorthalidone

Product NDC
72162-2133
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Chlorthalidone
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA212878
Marketing category
ANDA
Substance
CHLORTHALIDONE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
72162-2133-01000 TABLET in 1 BOTTLE (72162-2133-0) 2023-09-19NoHistorical
72162-2133-1100 TABLET in 1 BOTTLE (72162-2133-1) 2023-09-19NoHistorical
72162-2133-330 TABLET in 1 BOTTLE (72162-2133-3) 2023-09-19NoHistorical
72162-2133-660 TABLET in 1 BOTTLE (72162-2133-6) 2023-09-19NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Chlorthalidone Tablets, 25 mg and 50 mgBryant Ranch Prepack2025-01-29HUMAN PRESCRIPTION DRUG LABEL102