up and up nicotine (11673-411)

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 2 mg/1

Identifiers & Regulatory

Product NDC 11673-411

Product ID 11673-411_9d5a6785-f69e-44cb-ac46-963116a3df79

Product Type HUMAN OTC DRUG

Marketing Category ANDA

Application Number ANDA206394

Listing Expiration 2026-12-31

Marketing Start 2017-08-30

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 11673411

Hyphenated Format 11673-411

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 ANDA206394 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

2 mg/1

source: ndc

Packaging

160 BLISTER PACK in 1 CARTON (11673-411-06) / 1 GUM, CHEWING in 1 BLISTER PACK
20 BLISTER PACK in 1 CARTON (11673-411-60) / 1 GUM, CHEWING in 1 BLISTER PACK
100 BLISTER PACK in 1 CARTON (11673-411-78) / 1 GUM, CHEWING in 1 BLISTER PACK

source: ndc

Packages (3)

11673-411-06 160 BLISTER PACK in 1 CARTON (11673-411-06) / 1 GUM, CHEWING in 1 BLISTER PACK 11673-411-60 20 BLISTER PACK in 1 CARTON (11673-411-60) / 1 GUM, CHEWING in 1 BLISTER PACK 11673-411-78 100 BLISTER PACK in 1 CARTON (11673-411-78) / 1 GUM, CHEWING in 1 BLISTER PACK

Ingredients (1)

NICOTINE (2 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": "9d5a6785-f69e-44cb-ac46-963116a3df79", "openfda": {"nui": ["N0000175706", "M0014836"], "upc": ["0012345678905"], "unii": ["6M3C89ZY6R"], "rxcui": ["314119"], "spl_set_id": ["580b1def-25cc-4bdd-b80e-e2035b004808"], "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 (11673-411-06)  / 1 GUM, CHEWING in 1 BLISTER PACK", "package_ndc": "11673-411-06", "marketing_start_date": "20170831"}, {"sample": false, "description": "20 BLISTER PACK in 1 CARTON (11673-411-60)  / 1 GUM, CHEWING in 1 BLISTER PACK", "package_ndc": "11673-411-60", "marketing_start_date": "20170830"}, {"sample": false, "description": "100 BLISTER PACK in 1 CARTON (11673-411-78)  / 1 GUM, CHEWING in 1 BLISTER PACK", "package_ndc": "11673-411-78", "marketing_start_date": "20170831"}], "brand_name": "up and up nicotine", "product_id": "11673-411_9d5a6785-f69e-44cb-ac46-963116a3df79", "dosage_form": "GUM, CHEWING", "pharm_class": ["Cholinergic Nicotinic Agonist [EPC]", "Nicotine [CS]"], "product_ndc": "11673-411", "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": "2 mg/1"}], "application_number": "ANDA206394", "marketing_category": "ANDA", "marketing_start_date": "20170830", "listing_expiration_date": "20261231"}