Lidocaine Hydrochloride and Epinephrine

Product NDC

63739-475

11-digit product format

637390475

Labeler code

63739

Product ID

63739-475_3365c3d6-28a0-420d-89a7-9bc9b8539d4c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

lidocaine hydrochloride anhydrous and epinephrine

Dosage form

INJECTION, SOLUTION

Route

INFILTRATION

Labeler

McKesson Packaging Services Business Unit of McKesson Corporation

Application

ANDA089646

Marketing category

ANDA

Marketing start

2010-05-03

Marketing end

0000-00-00

Substance

LIDOCAINE HYDROCHLORIDE ANHYDROUS; EPINEPHRINE

Active strength

20 mg/mL; ug/mL

Pharmacologic classes

Amide Local Anesthetic [EPC],Amides [CS],Antiarrhythmic [EPC],Local Anesthesia [PE],Adrenergic alpha-Agonists [MoA],Adrenergic beta-Agonists [MoA],alpha-Adrenergic Agonist [EPC],beta-Adrenergic Agonist [EPC],Catecholamine [EPC],Catecholamines [CS]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record