In Control Nicotine

Product NDC
37808-352
11-digit product format
378080352
Labeler code
37808
Product ID
37808-352_8ccc1a17-cde4-4d9f-9a9d-d79e8a1b232d
Type
HUMAN OTC DRUG
Nonproprietary name
Nicotine Polacrilex
Dosage form
GUM, CHEWING
Route
ORAL
Labeler
H E B
Application
ANDA078547
Marketing category
ANDA
Marketing start
2007-12-13
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