in control nicotine

Product NDC

37808-170

11-digit product format

378080170

Labeler code

37808

Product ID

37808-170_e358414f-acbe-41c2-85f3-64da44fd0551

Type

HUMAN OTC DRUG

Nonproprietary name

Nicotine Polacrilex

Dosage form

GUM, CHEWING

Route

ORAL

Labeler

H E B

Application

ANDA076789

Marketing category

ANDA

Marketing start

2005-06-15

Marketing end

2021-01-01

Substance

NICOTINE

Active strength

4 mg/1

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record