HEALTHMART NICOTINE TRANSDERMAL SYSTEM

Product NDC

62011-0173

11-digit product format

620110173

Labeler code

62011

Product ID

62011-0173_089fb34b-60af-29f6-2ac3-4808f2cbbc6e

Type

HUMAN OTC DRUG

Nonproprietary name

NICOTINE

Dosage form

PATCH, EXTENDED RELEASE

Route

TOPICAL

Labeler

McKesson

Application

NDA020076

Marketing category

NDA

Marketing start

2015-08-14

Marketing end

0000-00-00

Substance

NICOTINE

Active strength

21 mg/24h

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record