Priloxx LP External Kit

Product NDC

51021-375

11-digit product format

510210375

Labeler code

51021

Product ID

51021-375_651bba60-a7f1-f48f-e053-2991aa0a1a88

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

lidocaine and prilocaine cream

Dosage form

KIT

Route

TOPICAL

Labeler

Sircle Laboratories LLC

Application

NDA019941

Marketing category

NDA

Marketing start

2017-05-20

Marketing end

0000-00-00

Active strength

0

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record