varenicline tartrate

Generic: varenicline tartrate

Labeler: florida pharmaceutical products, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name varenicline tartrate
Generic Name varenicline tartrate
Labeler florida pharmaceutical products, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

varenicline tartrate 1 mg/1

Manufacturer
Florida Pharmaceutical Products, LLC

Identifiers & Regulatory

Product NDC 71921-309
Product ID 71921-309_2b9c8b1e-6193-4d8e-9b50-6aca27294263
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA219106
Listing Expiration 2026-12-31
Marketing Start 2024-11-01

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 71921309
Hyphenated Format 71921-309

Supplemental Identifiers

RxCUI
636671 636676 749289
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 varenicline tartrate (source: ndc)
Generic Name varenicline tartrate (source: ndc)
Application Number ANDA219106 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 56 TABLET, FILM COATED in 1 BOTTLE (71921-309-56)
source: ndc

Packages (1)

71921-309-56 56 TABLET, FILM COATED in 1 BOTTLE (71921-309-56)

Ingredients (1)

varenicline tartrate (1 mg/1)

Linked Drug Pages (1)

Varenicline, Varenicline tartrate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2b9c8b1e-6193-4d8e-9b50-6aca27294263", "openfda": {"unii": ["82269ASB48"], "rxcui": ["636671", "636676", "749289"], "spl_set_id": ["2b9c8b1e-6193-4d8e-9b50-6aca27294263"], "manufacturer_name": ["Florida Pharmaceutical Products, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "56 TABLET, FILM COATED in 1 BOTTLE (71921-309-56)", "package_ndc": "71921-309-56", "marketing_start_date": "20241101"}], "brand_name": "Varenicline tartrate", "product_id": "71921-309_2b9c8b1e-6193-4d8e-9b50-6aca27294263", "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": "71921-309", "generic_name": "Varenicline tartrate", "labeler_name": "Florida Pharmaceutical Products, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Varenicline tartrate", "active_ingredients": [{"name": "VARENICLINE TARTRATE", "strength": "1 mg/1"}], "application_number": "ANDA219106", "marketing_category": "ANDA", "marketing_start_date": "20241101", "listing_expiration_date": "20261231"}