Nicorelief

Product NDC
50090-1145
11-digit product format
500901145
Labeler code
50090
Product ID
50090-1145_20201182-d7c5-4473-9d71-1b92f4b00fd7
Type
HUMAN OTC DRUG
Nonproprietary name
Nicotine Polacrilex
Dosage form
GUM, CHEWING
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA078325
Marketing category
ANDA
Marketing start
2005-04-12
Marketing end
0000-00-00
Substance
NICOTINE
Active strength
2 mg/1
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-1145-0EA - Each50090-1145a5265acf-8800-4cf4-9d07-f8a074c797f012018-11-06