Up and Up Nicotine

Generic: Nicotine Polacrilex

Labeler: Target Corporation
NDC Directory HUMAN OTC DRUG ANDA Inactive

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 11673-029
Product ID 11673-029_6b27678b-c83a-4dfb-a838-33720c48141f
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA076775
Marketing Start 2010-03-11
Marketing End 2026-03-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 11673029
Hyphenated Format 11673-029

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 ANDA076775 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 310 BLISTER PACK in 1 CARTON (11673-029-02) / 1 GUM, CHEWING in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (1)

NICOTINE (2 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6b27678b-c83a-4dfb-a838-33720c48141f", "openfda": {"nui": ["N0000175706", "M0014836"], "unii": ["6M3C89ZY6R"], "rxcui": ["314119"], "spl_set_id": ["82784eb7-da10-4933-8a21-cb3b831360aa"], "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": "310 BLISTER PACK in 1 CARTON (11673-029-02)  / 1 GUM, CHEWING in 1 BLISTER PACK", "package_ndc": "11673-029-02", "marketing_end_date": "20260301", "marketing_start_date": "20160317"}], "brand_name": "Up and Up Nicotine", "product_id": "11673-029_6b27678b-c83a-4dfb-a838-33720c48141f", "dosage_form": "GUM, CHEWING", "pharm_class": ["Cholinergic Nicotinic Agonist [EPC]", "Nicotine [CS]"], "product_ndc": "11673-029", "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": "ANDA076775", "marketing_category": "ANDA", "marketing_end_date": "20260301", "marketing_start_date": "20100311"}