Lidocaine Hydrochloride

Product NDC

70518-1098

11-digit product format

705181098

Labeler code

70518

Product ID

70518-1098_69855bbf-fc86-113d-e053-2a91aa0ac3cf

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

LIDOCAINE HYDROCHLORIDE

Dosage form

INJECTION, SOLUTION

Route

INFILTRATION; PERINEURAL

Labeler

REMEDYREPACK INC.

Application

ANDA088299

Marketing category

ANDA

Marketing start

2018-04-03

Marketing end

0000-00-00

Substance

LIDOCAINE HYDROCHLORIDE

Active strength

10 mg/mL

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record