sunmark nicotine

Product NDC
70677-0085
11-digit product format
706770085
Labeler code
70677
Product ID
70677-0085_21455933-e471-4a02-9e55-3c330f48973e
Type
HUMAN OTC DRUG
Nonproprietary name
Nicotine Polacrilex
Dosage form
GUM, CHEWING
Route
ORAL
Labeler
Strategic Sourcing Services LLC
Application
ANDA078547
Marketing category
ANDA
Marketing start
2019-12-07
Marketing end
0000-00-00
Substance
NICOTINE
Active strength
2 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
70677-0085-1EA - Each70677-0085326194a3-4f88-4c1f-ad8e-53b6bbd646e412021-04-08

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70677-0085SUNMARK NICOTINE (NICOTINE POLACRILEX) GUM, CHEWING [STRATEGIC SOURCING SERVICES LLC]4Legacy NDC20250228_0b252995-49ff-418f-8529-882d4a3fa31a.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70677-0085-170677008501100 BLISTER PACK in 1 CARTON (70677-0085-1) > 1 GUM, CHEWING in 1 BLISTER PACK100 blister pack2019-12-070000-00-00NoNoCurrent