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 LOZENGE
Routes
ORAL
Active Ingredients

nicotine 2 mg/1

Manufacturer
Walgreen Company

Identifiers & Regulatory

Product NDC 0363-0411
Product ID 0363-0411_4aba8ee5-d2b0-4f6d-ba98-03fb96877c50
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA077007
Listing Expiration 2026-12-31
Marketing Start 2006-02-23

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03630411
Hyphenated Format 0363-0411

Supplemental Identifiers

RxCUI
359817
UPC
0012345678905
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 ANDA077007 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 3 CONTAINER in 1 CARTON (0363-0411-05) / 24 LOZENGE in 1 CONTAINER
  • 4 CONTAINER in 1 CARTON (0363-0411-10) / 27 LOZENGE in 1 CONTAINER
  • 6 CONTAINER in 1 CARTON (0363-0411-16) / 24 LOZENGE in 1 CONTAINER
source: ndc

Packages (3)

Ingredients (1)

nicotine (2 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4aba8ee5-d2b0-4f6d-ba98-03fb96877c50", "openfda": {"nui": ["N0000175706", "M0014836"], "upc": ["0012345678905"], "unii": ["6M3C89ZY6R"], "rxcui": ["359817"], "spl_set_id": ["1123afbb-1785-43f0-aca4-dd5a9565d774"], "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": "3 CONTAINER in 1 CARTON (0363-0411-05)  / 24 LOZENGE in 1 CONTAINER", "package_ndc": "0363-0411-05", "marketing_start_date": "20100623"}, {"sample": false, "description": "4 CONTAINER in 1 CARTON (0363-0411-10)  / 27 LOZENGE in 1 CONTAINER", "package_ndc": "0363-0411-10", "marketing_start_date": "20130222"}, {"sample": false, "description": "6 CONTAINER in 1 CARTON (0363-0411-16)  / 24 LOZENGE in 1 CONTAINER", "package_ndc": "0363-0411-16", "marketing_start_date": "20151008"}], "brand_name": "Nicotine", "product_id": "0363-0411_4aba8ee5-d2b0-4f6d-ba98-03fb96877c50", "dosage_form": "LOZENGE", "pharm_class": ["Cholinergic Nicotinic Agonist [EPC]", "Nicotine [CS]"], "product_ndc": "0363-0411", "generic_name": "Nicotine Polacrilex", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Nicotine", "active_ingredients": [{"name": "NICOTINE", "strength": "2 mg/1"}], "application_number": "ANDA077007", "marketing_category": "ANDA", "marketing_start_date": "20060223", "listing_expiration_date": "20261231"}