Nadolol

Product NDC
71335-2131
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Nadolol
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA210955
Marketing category
ANDA
Substance
NADOLOL
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
71335-2131-228 TABLET in 1 BOTTLE (71335-2131-2) 20240403NoHistorical

Related DailyMed Labels

Set IDTitleManufacturerEffective dateTypeVersion
c154d99c-e4fb-41d0-8fac-e1982672e8d7Nadolol Tablets, USPBryant Ranch Prepack2024-04-03HUMAN PRESCRIPTION DRUG LABEL102