LIDOCAINE

Product NDC

50742-306

11-digit product format

507420306

Labeler code

50742

Product ID

50742-306_de1ea59d-baee-4723-9caf-8c56b6b94fd3

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Lidocaine

Dosage form

OINTMENT

Route

TOPICAL

Labeler

Ingenus Pharmaceuticals, LLC

Application

ANDA208604

Marketing category

ANDA

Marketing start

2017-09-20

Marketing end

0000-00-00

Substance

LIDOCAINE

Active strength

50 mg/g

Pharmacologic classes

Amide Local Anesthetic [EPC],Amides [CS],Antiarrhythmic [EPC],Local Anesthesia [PE]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record