varenicline

Generic: varenicline tartrate

Labeler: camber pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name varenicline
Generic Name varenicline tartrate
Labeler camber pharmaceuticals, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

varenicline tartrate .5 mg/1

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-678
Product ID 31722-678_09a2708f-ed1b-b986-e063-6394a90a8fb5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214571
Listing Expiration 2026-12-31
Marketing Start 2023-10-23

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 31722678
Hyphenated Format 31722-678

Supplemental Identifiers

RxCUI
636671 636676 749289 749788
UPC
0331722678568 0331722679565
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 ANDA214571 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .5 mg/1
source: ndc
Packaging
  • 56 TABLET, FILM COATED in 1 BOTTLE (31722-678-56)
source: ndc

Packages (1)

31722-678-56 56 TABLET, FILM COATED in 1 BOTTLE (31722-678-56)

Ingredients (1)

varenicline tartrate (.5 mg/1)

Linked Drug Pages (1)

Varenicline ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "09a2708f-ed1b-b986-e063-6394a90a8fb5", "openfda": {"upc": ["0331722678568", "0331722679565"], "unii": ["82269ASB48"], "rxcui": ["636671", "636676", "749289", "749788"], "spl_set_id": ["7bd1abc8-2689-496b-b3f2-1cefe218ff5a"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "56 TABLET, FILM COATED in 1 BOTTLE (31722-678-56)", "package_ndc": "31722-678-56", "marketing_start_date": "20231023"}], "brand_name": "Varenicline", "product_id": "31722-678_09a2708f-ed1b-b986-e063-6394a90a8fb5", "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": "31722-678", "generic_name": "Varenicline tartrate", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Varenicline", "active_ingredients": [{"name": "VARENICLINE TARTRATE", "strength": ".5 mg/1"}], "application_number": "ANDA214571", "marketing_category": "ANDA", "marketing_start_date": "20231023", "listing_expiration_date": "20261231"}