chantix

Generic: varenicline tartrate

Labeler: pfizer laboratories div pfizer inc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name chantix
Generic Name varenicline tartrate
Labeler pfizer laboratories div pfizer inc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

varenicline tartrate 1 mg/1

Manufacturer
Pfizer Laboratories Div Pfizer Inc

Identifiers & Regulatory

Product NDC 0069-0469
Product ID 0069-0469_09cce88b-e4f0-48b7-ac05-54d97976b4c5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA021928
Listing Expiration 2027-12-31
Marketing Start 2006-05-10

Pharmacologic Class

Classes
cholinergic agonists [moa] cholinergic receptor agonist [epc] partial cholinergic nicotinic agonist [epc] partial cholinergic nicotinic agonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00690469
Hyphenated Format 0069-0469

Supplemental Identifiers

RxCUI
636671 636676 637188 637190 749289 749788 795735 795737
UPC
0300690469560 0300690468563 0300690471280
UNII
82269ASB48

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 chantix (source: ndc)
Generic Name varenicline tartrate (source: ndc)
Application Number NDA021928 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 56 TABLET, FILM COATED in 1 BLISTER PACK (0069-0469-28)
  • 56 TABLET, FILM COATED in 1 BOTTLE (0069-0469-56)
source: ndc

Packages (2)

0069-0469-28 56 TABLET, FILM COATED in 1 BLISTER PACK (0069-0469-28) 0069-0469-56 56 TABLET, FILM COATED in 1 BOTTLE (0069-0469-56)

Ingredients (1)

varenicline tartrate (1 mg/1)

Linked Drug Pages (1)

CHANTIX ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "09cce88b-e4f0-48b7-ac05-54d97976b4c5", "openfda": {"upc": ["0300690469560", "0300690468563", "0300690471280"], "unii": ["82269ASB48"], "rxcui": ["636671", "636676", "637188", "637190", "749289", "749788", "795735", "795737"], "spl_set_id": ["f0ff4f27-5185-4881-a749-c6b7a0ca5696"], "manufacturer_name": ["Pfizer Laboratories Div Pfizer Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "56 TABLET, FILM COATED in 1 BLISTER PACK (0069-0469-28)", "package_ndc": "0069-0469-28", "marketing_start_date": "20250922"}, {"sample": false, "description": "56 TABLET, FILM COATED in 1 BOTTLE (0069-0469-56)", "package_ndc": "0069-0469-56", "marketing_start_date": "20060510"}], "brand_name": "CHANTIX", "product_id": "0069-0469_09cce88b-e4f0-48b7-ac05-54d97976b4c5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinergic Agonists [MoA]", "Cholinergic Receptor Agonist [EPC]", "Partial Cholinergic Nicotinic Agonist [EPC]", "Partial Cholinergic Nicotinic Agonists [MoA]"], "product_ndc": "0069-0469", "generic_name": "varenicline tartrate", "labeler_name": "Pfizer Laboratories Div Pfizer Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CHANTIX", "active_ingredients": [{"name": "VARENICLINE TARTRATE", "strength": "1 mg/1"}], "application_number": "NDA021928", "marketing_category": "NDA", "marketing_start_date": "20060510", "listing_expiration_date": "20271231"}