Felodipine

Product NDC
50090-1124
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Felodipine
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA202170
Marketing category
ANDA
Substance
FELODIPINE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-1124-030 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-1124-0) 2014-11-28NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Felodipine Extended-Release Tablets, USP Rx onlyA-S Medication Solutions2025-01-22HUMAN PRESCRIPTION DRUG LABEL4