NICOTINE

Product NDC

49781-142

11-digit product format

497810142

Labeler code

49781

Product ID

49781-142_31fda3d5-e812-bc1b-6ae6-5f40462e5a90

Type

HUMAN OTC DRUG

Nonproprietary name

NICOTINE

Dosage form

PATCH, EXTENDED RELEASE

Route

TRANSDERMAL

Labeler

Cardinal Health (Leader)

Application

NDA020076

Marketing category

NDA

Marketing start

2015-10-01

Marketing end

0000-00-00

Substance

NICOTINE

Active strength

21 mg/24h

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record