up and up nicotine (11673-309)

Drug Facts

Product Profile

Brand Name up and up nicotine

Generic Name nicotine polacrilex

Labeler target corporation

Dosage Form GUM, CHEWING

Routes

ORAL

Active Ingredients

nicotine 4 mg/1

Manufacturer

Target Corporation

Identifiers & Regulatory

Product NDC 11673-309

Product ID 11673-309_4ad3680c-f184-474d-914c-397aad146e82

Product Type HUMAN OTC DRUG

Marketing Category ANDA

Application Number ANDA206393

Listing Expiration 2026-12-31

Marketing Start 2017-08-31

Pharmacologic Class

Established (EPC)

cholinergic nicotinic agonist [epc]

Chemical Structure

nicotine [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 11673309

Hyphenated Format 11673-309

Supplemental Identifiers

RxCUI

311975

UNII

6M3C89ZY6R

NUI

N0000175706 M0014836

Packaging Origin

Original Packager

true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name up and up nicotine (source: ndc)

Generic Name nicotine polacrilex (source: ndc)

Application Number ANDA206393 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

4 mg/1

source: ndc

Packaging

160 BLISTER PACK in 1 CARTON (11673-309-06) / 1 GUM, CHEWING in 1 BLISTER PACK
20 BLISTER PACK in 1 CARTON (11673-309-60) / 1 GUM, CHEWING in 1 BLISTER PACK
100 BLISTER PACK in 1 CARTON (11673-309-78) / 1 GUM, CHEWING in 1 BLISTER PACK

source: ndc

Packages (3)

11673-309-06 160 BLISTER PACK in 1 CARTON (11673-309-06) / 1 GUM, CHEWING in 1 BLISTER PACK 11673-309-60 20 BLISTER PACK in 1 CARTON (11673-309-60) / 1 GUM, CHEWING in 1 BLISTER PACK 11673-309-78 100 BLISTER PACK in 1 CARTON (11673-309-78) / 1 GUM, CHEWING in 1 BLISTER PACK

Ingredients (1)

nicotine (4 mg/1)

Linked Drug Pages (1)

Up and Up Nicotine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "4ad3680c-f184-474d-914c-397aad146e82", "openfda": {"nui": ["N0000175706", "M0014836"], "unii": ["6M3C89ZY6R"], "rxcui": ["311975"], "spl_set_id": ["d59c804f-33ab-4a46-b112-e7752f383f7f"], "pharm_class_cs": ["Nicotine [CS]"], "pharm_class_epc": ["Cholinergic Nicotinic Agonist [EPC]"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "160 BLISTER PACK in 1 CARTON (11673-309-06)  / 1 GUM, CHEWING in 1 BLISTER PACK", "package_ndc": "11673-309-06", "marketing_start_date": "20170831"}, {"sample": false, "description": "20 BLISTER PACK in 1 CARTON (11673-309-60)  / 1 GUM, CHEWING in 1 BLISTER PACK", "package_ndc": "11673-309-60", "marketing_start_date": "20170831"}, {"sample": false, "description": "100 BLISTER PACK in 1 CARTON (11673-309-78)  / 1 GUM, CHEWING in 1 BLISTER PACK", "package_ndc": "11673-309-78", "marketing_start_date": "20170831"}], "brand_name": "Up and Up Nicotine", "product_id": "11673-309_4ad3680c-f184-474d-914c-397aad146e82", "dosage_form": "GUM, CHEWING", "pharm_class": ["Cholinergic Nicotinic Agonist [EPC]", "Nicotine [CS]"], "product_ndc": "11673-309", "generic_name": "Nicotine Polacrilex", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Up and Up Nicotine", "active_ingredients": [{"name": "NICOTINE", "strength": "4 mg/1"}], "application_number": "ANDA206393", "marketing_category": "ANDA", "marketing_start_date": "20170831", "listing_expiration_date": "20261231"}