varenicline

Generic: varenicline tartrate

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

Drug Facts

Product Profile

Brand Name varenicline
Generic Name varenicline tartrate
Labeler florida pharmaceutical products, llc
Dosage Form KIT
Manufacturer
Florida Pharmaceutical Products, LLC

Identifiers & Regulatory

Product NDC 71921-307
Product ID 71921-307_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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71921307
Hyphenated Format 71921-307

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 (source: ndc)
Generic Name varenicline tartrate (source: ndc)
Application Number ANDA219106 (source: ndc)
Routes
oral
source: label

Resolved Composition

Strengths
  • 0.5 mg
  • 1 mg
source: label
Packaging
  • 1 KIT in 1 CARTON (71921-307-51) * 11 TABLET, FILM COATED in 1 BLISTER PACK * 42 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (1)

71921-307-51 1 KIT in 1 CARTON (71921-307-51) * 11 TABLET, FILM COATED in 1 BLISTER PACK * 42 TABLET, FILM COATED in 1 BLISTER PACK

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Varenicline, Varenicline tartrate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"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": "1 KIT in 1 CARTON (71921-307-51)  *  11 TABLET, FILM COATED in 1 BLISTER PACK *  42 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "71921-307-51", "marketing_start_date": "20241101"}], "brand_name": "Varenicline", "product_id": "71921-307_2b9c8b1e-6193-4d8e-9b50-6aca27294263", "dosage_form": "KIT", "product_ndc": "71921-307", "generic_name": "Varenicline Tartrate", "labeler_name": "Florida Pharmaceutical Products, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Varenicline", "application_number": "ANDA219106", "marketing_category": "ANDA", "marketing_start_date": "20241101", "listing_expiration_date": "20261231"}