In Control Nicotine

Product NDC
37808-309
11-digit product format
378080309
Labeler code
37808
Product ID
37808-309_8a5e5db5-19a9-4743-8a35-9af269d82e4e
Type
HUMAN OTC DRUG
Nonproprietary name
Nicotine Polacrilex
Dosage form
GUM, CHEWING
Route
ORAL
Labeler
H E B
Application
ANDA206393
Marketing category
ANDA
Marketing start
2017-01-23
Marketing end
0000-00-00
Substance
NICOTINE
Active strength
4 mg/1
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record