tolterodine tartrate

Generic: tolterodine tartrate

Labeler: mylan pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

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

tolterodine tartrate 2 mg/1

Manufacturer
Mylan Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 59762-0800
Product ID 59762-0800_fdede630-529a-48fe-b796-59c3504c8d32
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA020771
Marketing Start 2014-01-21
Marketing End 2026-07-31

Pharmacologic Class

Classes
cholinergic muscarinic antagonist [epc] cholinergic muscarinic antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 597620800
Hyphenated Format 59762-0800

Supplemental Identifiers

RxCUI
855178 855194
UPC
0359762017062 0359762080028
UNII
5T619TQR3R

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 tolterodine tartrate (source: ndc)
Generic Name tolterodine tartrate (source: ndc)
Application Number NDA020771 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 60 TABLET, FILM COATED in 1 BOTTLE (59762-0800-2)
  • 500 TABLET, FILM COATED in 1 BOTTLE (59762-0800-6)
source: ndc

Packages (2)

59762-0800-2 60 TABLET, FILM COATED in 1 BOTTLE (59762-0800-2) 59762-0800-6 500 TABLET, FILM COATED in 1 BOTTLE (59762-0800-6)

Ingredients (1)

tolterodine tartrate (2 mg/1)

Linked Drug Pages (1)

Tolterodine Tartrate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "fdede630-529a-48fe-b796-59c3504c8d32", "openfda": {"upc": ["0359762017062", "0359762080028"], "unii": ["5T619TQR3R"], "rxcui": ["855178", "855194"], "spl_set_id": ["9e432622-2e6f-4cf8-892f-510288dd50f2"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (59762-0800-2)", "package_ndc": "59762-0800-2", "marketing_end_date": "20260630", "marketing_start_date": "20140121"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (59762-0800-6)", "package_ndc": "59762-0800-6", "marketing_end_date": "20260731", "marketing_start_date": "20140121"}], "brand_name": "Tolterodine Tartrate", "product_id": "59762-0800_fdede630-529a-48fe-b796-59c3504c8d32", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "59762-0800", "generic_name": "Tolterodine Tartrate", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tolterodine Tartrate", "active_ingredients": [{"name": "TOLTERODINE TARTRATE", "strength": "2 mg/1"}], "application_number": "NDA020771", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_end_date": "20260731", "marketing_start_date": "20140121"}