Rocuronium Bromide

Product NDC

0703-2395

11-digit product format

007032395

Labeler code

0703

Product ID

0703-2395_5f3aa05d-26c6-48fc-9a2c-dc0118d020a4

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Rocuronium Bromide

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS

Labeler

Teva Parenteral Medicines

Application

ANDA078717

Marketing category

ANDA

Marketing start

2008-12-01

Marketing end

0000-00-00

Substance

ROCURONIUM BROM

Active strength

10 mg/mL

Pharmacologic classes

Neuromuscular N

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record