in control nicotine

Product NDC

37808-734

11-digit product format

378080734

Labeler code

37808

Product ID

37808-734_21221f3d-f617-4ae8-a363-1fb2b2952798

Type

HUMAN OTC DRUG

Nonproprietary name

Nicotine Polacrilex

Dosage form

LOZENGE

Route

ORAL

Labeler

H E B

Application

ANDA203690

Marketing category

ANDA

Marketing start

2014-07-23

Marketing end

0000-00-00

Substance

NICOTINE

Active strength

2 mg/1

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record