Atracurium Besylate

Product NDC

65862-984

11-digit product format

658620984

Labeler code

65862

Product ID

65862-984_5176be07-3121-49fb-9eb9-638903753a31

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Atracurium Besylate

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS

Labeler

Aurobindo Pharma Limited

Application

ANDA206010

Marketing category

ANDA

Marketing start

2015-04-08

Marketing end

0000-00-00

Substance

ATRACURIUM BESYLATE

Active strength

50 mg/5mL

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record