sunmark nicotine

Product NDC
70677-0170
11-digit product format
706770170
Labeler code
70677
Product ID
70677-0170_29ae0e2a-9161-491e-8f9f-65e83717ed64
Type
HUMAN OTC DRUG
Nonproprietary name
nicotine polacrilex
Dosage form
GUM, CHEWING
Route
ORAL
Labeler
Strategic Sourcing Services LLC
Application
ANDA206393
Marketing category
ANDA
Marketing start
2022-12-15
Marketing end
0000-00-00
Substance
NICOTINE
Active strength
4 mg/1
Pharmacologic classes
Cholinergic Nicotinic Agonist [EPC], Nicotine [CS]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70677-0170-1EA - Each70677-01703e7706a1-ada7-44b6-859e-94e44c7ed28912024-08-12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70677-0170SUNMARK NICOTINE (NICOTINE POLACRILEX) GUM, CHEWING [STRATEGIC SOURCING SERVICES LLC]2Legacy NDC20230620_29ae0e2a-9161-491e-8f9f-65e83717ed64.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70677-0170-070677017000110 BLISTER PACK in 1 CARTON (70677-0170-0) > 1 GUM, CHEWING in 1 BLISTER PACK110 blister pack2022-12-150000-00-00NoNoCurrent