Nicotine

Product NDC
30142-854
11-digit product format
301420854
Labeler code
30142
Product ID
30142-854_6916b403-a5d9-4bec-97bc-d31d4a857728
Type
HUMAN OTC DRUG
Nonproprietary name
Nicotine polacrilex
Dosage form
GUM, CHEWING
Route
ORAL
Labeler
Kroger Company
Application
ANDA078546
Marketing category
ANDA
Marketing start
2007-09-15
Marketing end
0000-00-00
Substance
NICOTINE
Active strength
4 mg/1
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
30142-854-78EA - Each30142-854688c20b7-9e87-420b-a588-979097d43de312016-03-04

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
30142-854-0630142085406160 BLISTER PACK in 1 CARTON (30142-854-06) > 1 GUM, CHEWING in 1 BLISTER PACK160 blister pack2016-03-090000-00-00NoNoCurrent
30142-854-603014208546020 BLISTER PACK in 1 CARTON (30142-854-60) > 1 GUM, CHEWING in 1 BLISTER PACK20 blister pack2011-04-110000-00-00NoNoCurrent
30142-854-7630142085476120 BLISTER PACK in 1 CARTON (30142-854-76) > 1 GUM, CHEWING in 1 BLISTER PACK120 blister pack2008-04-070000-00-00NoNoCurrent
30142-854-7830142085478100 BLISTER PACK in 1 CARTON (30142-854-78) > 1 GUM, CHEWING in 1 BLISTER PACK100 blister pack2007-09-150000-00-00NoNoCurrent