In Control Nicotine

Product NDC

37808-532

11-digit product format

378080532

Labeler code

37808

Product ID

37808-532_c2bef107-71ee-46a1-aba3-2475a9bc8fbe

Type

HUMAN OTC DRUG

Nonproprietary name

Nicotine Polacrilex

Dosage form

GUM, CHEWING

Route

ORAL

Labeler

H E B

Application

ANDA076779

Marketing category

ANDA

Marketing start

2006-10-13

Marketing end

2021-02-01

Substance

NICOTINE

Active strength

4 mg/1

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record