hydrochlorothiazide

Product NDC
50090-0724
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
hydrochlorothiazide
Dosage form
CAPSULE
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA090510
Marketing category
ANDA
Substance
HYDROCHLOROTHIAZIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-0724-030 CAPSULE in 1 BOTTLE (50090-0724-0) 2014-11-28NoHistorical
50090-0724-1100 CAPSULE in 1 BOTTLE (50090-0724-1) 2014-11-28NoHistorical
50090-0724-260 CAPSULE in 1 BOTTLE (50090-0724-2) 2014-11-28NoHistorical
50090-0724-390 CAPSULE in 1 BOTTLE (50090-0724-3) 2014-11-28NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Hydrochlorothiazide Capsules USP, 12.5 mgA-S Medication Solutions2024-04-11HUMAN PRESCRIPTION DRUG LABEL15