Dabigatran Etexilate

Product NDC
50090-7656
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Dabigatran Etexilate
Dosage form
CAPSULE, COATED PELLETS
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA208040
Marketing category
ANDA
Substance
DABIGATRAN ETEXILATE MESYLATE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-7656-060 CAPSULE, COATED PELLETS in 1 BOTTLE (50090-7656-0) 2025-09-18NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Dabigatran EtexilateA-S Medication Solutions2025-09-22Human Prescription Drug Label1