detrol

Generic: tolterodine tartrate

Labeler: viatris specialty llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name detrol
Generic Name tolterodine tartrate
Labeler viatris specialty llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

tolterodine tartrate 1 mg/1

Manufacturer
Viatris Specialty LLC

Identifiers & Regulatory

Product NDC 58151-098
Product ID 58151-098_f27726af-7a9b-45f4-96e0-1e90a5fdcc18
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA020771
Marketing Start 2024-05-21
Marketing End 2026-08-31

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 58151098
Hyphenated Format 58151-098

Supplemental Identifiers

RxCUI
855178 855180 855194 855195
UPC
0358151098910 0358151099917
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 detrol (source: ndc)
Generic Name tolterodine tartrate (source: ndc)
Application Number NDA020771 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 60 TABLET, FILM COATED in 1 BOTTLE (58151-098-91)
source: ndc

Packages (1)

58151-098-91 60 TABLET, FILM COATED in 1 BOTTLE (58151-098-91)

Ingredients (1)

tolterodine tartrate (1 mg/1)

Linked Drug Pages (1)

Detrol ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f27726af-7a9b-45f4-96e0-1e90a5fdcc18", "openfda": {"upc": ["0358151098910", "0358151099917"], "unii": ["5T619TQR3R"], "rxcui": ["855178", "855180", "855194", "855195"], "spl_set_id": ["41eb00d2-64e3-4ec9-8732-4bfc81b04180"], "manufacturer_name": ["Viatris Specialty LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (58151-098-91)", "package_ndc": "58151-098-91", "marketing_end_date": "20260831", "marketing_start_date": "20240521"}], "brand_name": "Detrol", "product_id": "58151-098_f27726af-7a9b-45f4-96e0-1e90a5fdcc18", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "58151-098", "generic_name": "tolterodine tartrate", "labeler_name": "Viatris Specialty LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Detrol", "active_ingredients": [{"name": "TOLTERODINE TARTRATE", "strength": "1 mg/1"}], "application_number": "NDA020771", "marketing_category": "NDA", "marketing_end_date": "20260831", "marketing_start_date": "20240521"}