Vecuronium

Product NDC

25021-658

11-digit product format

250210658

Labeler code

25021

Product ID

25021-658_97234f4c-7033-4a5b-bf1c-6db579cd37bf

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

vecuronium bromide

Dosage form

INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Route

INTRAVENOUS

Labeler

Sagent Pharmaceuticals

Application

ANDA078274

Marketing category

ANDA

Marketing start

2011-08-01

Marketing end

0000-00-00

Substance

VECURONIUM BROMIDE

Active strength

20 mg/20mL

Pharmacologic classes

Neuromuscular Nondepolarizing Blockade [PE],Nondepolarizing Neuromuscular Blocker [EPC]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record