tolterodine tartrate

Generic: tolterodine tartrate

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

Drug Facts

Product Profile

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

tolterodine tartrate 2 mg/1

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0093-0018
Product ID 0093-0018_2f429822-d6d2-43c0-9aaf-1270b3e92a2f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077006
Listing Expiration 2026-12-31
Marketing Start 2015-11-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00930018
Hyphenated Format 0093-0018

Supplemental Identifiers

RxCUI
855178 855194
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 ANDA077006 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 500 TABLET, FILM COATED in 1 BOTTLE (0093-0018-05)
  • 60 TABLET, FILM COATED in 1 BOTTLE (0093-0018-06)
source: ndc

Packages (2)

0093-0018-05 500 TABLET, FILM COATED in 1 BOTTLE (0093-0018-05) 0093-0018-06 60 TABLET, FILM COATED in 1 BOTTLE (0093-0018-06)

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": "2f429822-d6d2-43c0-9aaf-1270b3e92a2f", "openfda": {"unii": ["5T619TQR3R"], "rxcui": ["855178", "855194"], "spl_set_id": ["d27e25b5-5d02-419f-b098-41fb162c5872"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (0093-0018-05)", "package_ndc": "0093-0018-05", "marketing_start_date": "20151101"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (0093-0018-06)", "package_ndc": "0093-0018-06", "marketing_start_date": "20151101"}], "brand_name": "Tolterodine Tartrate", "product_id": "0093-0018_2f429822-d6d2-43c0-9aaf-1270b3e92a2f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "0093-0018", "generic_name": "Tolterodine Tartrate", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tolterodine Tartrate", "active_ingredients": [{"name": "TOLTERODINE TARTRATE", "strength": "2 mg/1"}], "application_number": "ANDA077006", "marketing_category": "ANDA", "marketing_start_date": "20151101", "listing_expiration_date": "20261231"}