Pioglitazone

Product NDC
50090-6873
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Pioglitazone
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA202467
Marketing category
ANDA
Substance
PIOGLITAZONE HYDROCHLORIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-6873-030 TABLET in 1 BOTTLE (50090-6873-0) 2023-12-04NoHistorical
50090-6873-190 TABLET in 1 BOTTLE (50090-6873-1) 2023-12-04NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
PioglitazoneA-S Medication Solutions2023-12-05Human Prescription Drug Label1