Nadolol

Product NDC
72162-2233
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Nadolol
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA203455
Marketing category
ANDA
Substance
NADOLOL
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
72162-2233-1100 TABLET in 1 BOTTLE (72162-2233-1) 2024-01-26NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Rx OnlyBryant Ranch Prepack2024-01-26HUMAN PRESCRIPTION DRUG LABEL100