nicotine

Generic: nicotine polacrilex

Labeler: walgreen company
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nicotine
Generic Name nicotine polacrilex
Labeler walgreen company
Dosage Form GUM, CHEWING
Routes
ORAL
Active Ingredients

nicotine 4 mg/1

Manufacturer
Walgreen Company

Identifiers & Regulatory

Product NDC 0363-0919
Product ID 0363-0919_e12ce261-60f8-40cf-9c72-eba0cb659136
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA076779
Listing Expiration 2026-12-31
Marketing Start 2014-03-18

Pharmacologic Class

Established (EPC)
cholinergic nicotinic agonist [epc]
Chemical Structure
nicotine [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03630919
Hyphenated Format 0363-0919

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 nicotine (source: ndc)
Generic Name nicotine polacrilex (source: ndc)
Application Number ANDA076779 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/1
source: ndc
Packaging
  • 160 BLISTER PACK in 1 CARTON (0363-0919-06) / 1 GUM, CHEWING in 1 BLISTER PACK
  • 20 BLISTER PACK in 1 CARTON (0363-0919-60) / 1 GUM, CHEWING in 1 BLISTER PACK
  • 100 BLISTER PACK in 1 CARTON (0363-0919-78) / 1 GUM, CHEWING in 1 BLISTER PACK
source: ndc

Packages (3)

Ingredients (1)

nicotine (4 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e12ce261-60f8-40cf-9c72-eba0cb659136", "openfda": {"nui": ["N0000175706", "M0014836"], "unii": ["6M3C89ZY6R"], "rxcui": ["311975"], "spl_set_id": ["c44821ba-5c2a-4586-8210-afc02a4031d5"], "pharm_class_cs": ["Nicotine [CS]"], "pharm_class_epc": ["Cholinergic Nicotinic Agonist [EPC]"], "manufacturer_name": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "160 BLISTER PACK in 1 CARTON (0363-0919-06)  / 1 GUM, CHEWING in 1 BLISTER PACK", "package_ndc": "0363-0919-06", "marketing_start_date": "20180131"}, {"sample": false, "description": "20 BLISTER PACK in 1 CARTON (0363-0919-60)  / 1 GUM, CHEWING in 1 BLISTER PACK", "package_ndc": "0363-0919-60", "marketing_start_date": "20140318"}, {"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0363-0919-78)  / 1 GUM, CHEWING in 1 BLISTER PACK", "package_ndc": "0363-0919-78", "marketing_start_date": "20140318"}], "brand_name": "Nicotine", "product_id": "0363-0919_e12ce261-60f8-40cf-9c72-eba0cb659136", "dosage_form": "GUM, CHEWING", "pharm_class": ["Cholinergic Nicotinic Agonist [EPC]", "Nicotine [CS]"], "product_ndc": "0363-0919", "generic_name": "Nicotine polacrilex", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Nicotine", "active_ingredients": [{"name": "NICOTINE", "strength": "4 mg/1"}], "application_number": "ANDA076779", "marketing_category": "ANDA", "marketing_start_date": "20140318", "listing_expiration_date": "20261231"}