Anectine

Product NDC

0781-3009

11-digit product format

007813009

Labeler code

0781

Product ID

0781-3009_a90af0a9-4e44-4f19-ae41-561b4392bf02

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Succinylcholine Chloride

Dosage form

INJECTION, SOLUTION

Route

INTRAMUSCULAR; INTRAVENOUS; PARENTERAL

Labeler

Sandoz Inc

Application

NDA008453

Marketing category

NDA

Marketing start

1952-08-20

Marketing end

2019-05-31

Substance

SUCCINYLCHOLINE CHLORIDE

Active strength

20 mg/mL

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record