ROPIVACAINE HYDROCHLORIDE

Product NDC
67457-799
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
ROPIVACAINE HYDROCHLORIDE
Dosage form
INJECTION, SOLUTION
Route
EPIDURAL; INFILTRATION; PERINEURAL
Labeler
Mylan Institutional LLC
Application
ANDA206091
Marketing category
ANDA
Substance
ROPIVACAINE HYDROCHLORIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
67457-799-9910 POUCH in 1 CARTON (67457-799-99) / 1 BAG in 1 POUCH (67457-799-20) / 200 mL in 1 BAG2024-03-18NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
ROPIVACAINE HYDROCHLORIDEMylan Institutional LLC2023-12-15HUMAN PRESCRIPTION DRUG LABEL1