Tramadol HCL ER

Product NDC
72189-521
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Tramadol HCL ER
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
Direct_Rx
Application
ANDA200503
Marketing category
ANDA
Substance
TRAMADOL HYDROCHLORIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
72189-521-3030 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-521-30) 2023-11-08NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Tramadol HCL ER C-IVDirect_Rx2025-01-22HUMAN PRESCRIPTION DRUG LABEL2