varenicline tartrate
Generic: varenicline tartrate
Labeler: leading pharma, llcDrug Facts
Product Profile
Brand Name
varenicline tartrate
Generic Name
varenicline tartrate
Labeler
leading pharma, llc
Dosage Form
KIT
Manufacturer
Identifiers & Regulatory
Product NDC
69315-404
Product ID
69315-404_cd15d74e-92d3-4bf0-8c76-a01f9190b172
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA217151
Listing Expiration
2026-12-31
Marketing Start
2023-10-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69315404
Hyphenated Format
69315-404
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
ANDA217151 (source: ndc)
Routes
source: label
Resolved Composition
Strengths
- 0.5 mg
- 1 mg
Packaging
- 1 KIT in 1 BOX (69315-404-57) * 11 TABLET, FILM COATED in 1 BLISTER PACK * 42 TABLET, FILM COATED in 1 BLISTER PACK
Packages (1)
Ingredients (0)
No ingredient records.
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "cd15d74e-92d3-4bf0-8c76-a01f9190b172", "openfda": {"upc": ["0369315403563", "0369315402566"], "unii": ["82269ASB48"], "rxcui": ["636671", "636676", "749289", "749788"], "spl_set_id": ["fdb36cfa-d20a-4fd9-b994-a5d16e4bb438"], "manufacturer_name": ["Leading Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 BOX (69315-404-57) * 11 TABLET, FILM COATED in 1 BLISTER PACK * 42 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "69315-404-57", "marketing_start_date": "20231001"}], "brand_name": "VARENICLINE TARTRATE", "product_id": "69315-404_cd15d74e-92d3-4bf0-8c76-a01f9190b172", "dosage_form": "KIT", "product_ndc": "69315-404", "generic_name": "VARENICLINE TARTRATE", "labeler_name": "Leading Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VARENICLINE TARTRATE", "application_number": "ANDA217151", "marketing_category": "ANDA", "marketing_start_date": "20231001", "listing_expiration_date": "20261231"}