Meijer NICOTINE TRANSDERMAL SYSTEM

Product NDC

0067-6013

11-digit product format

000676013

Labeler code

0067

Product ID

0067-6013_e6681e9d-cde2-4184-b76f-bf7b01a6f8bc

Type

HUMAN OTC DRUG

Nonproprietary name

NICOTINE

Dosage form

PATCH, EXTENDED RELEASE

Route

TOPICAL

Labeler

Novartis Consumer Health

Application

NDA020076

Marketing category

NDA

Marketing start

2007-11-05

Marketing end

0000-00-00

Substance

NICOTINE

Active strength

21 mg/1

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record