Rocuronium

Product NDC
72162-2263
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Rocuronium
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Labeler
Bryant Ranch Prepack
Application
ANDA210437
Marketing category
ANDA
Substance
ROCURONIUM BROMIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
72162-2263-210 VIAL in 1 CARTON (72162-2263-2) / 5 mL in 1 VIAL2024-02-23NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
RocuroniumBryant Ranch Prepack2026-03-03HUMAN PRESCRIPTION DRUG LABEL101