tolterodine tartrate

Generic: tolterodine tartrate

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name tolterodine tartrate
Generic Name tolterodine tartrate
Labeler proficient rx lp
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

tolterodine tartrate 1 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-319
Product ID 71205-319_df5371c1-a1d3-4e6d-af7a-17cb46d7653d
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 71205319
Hyphenated Format 71205-319

Supplemental Identifiers

RxCUI
855178
UNII
5T619TQR3R

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
  • 1 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (71205-319-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71205-319-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71205-319-90)
source: ndc

Packages (3)

71205-319-30 30 TABLET, FILM COATED in 1 BOTTLE (71205-319-30) 71205-319-60 60 TABLET, FILM COATED in 1 BOTTLE (71205-319-60) 71205-319-90 90 TABLET, FILM COATED in 1 BOTTLE (71205-319-90)

Ingredients (1)

tolterodine tartrate (1 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": "df5371c1-a1d3-4e6d-af7a-17cb46d7653d", "openfda": {"unii": ["5T619TQR3R"], "rxcui": ["855178"], "spl_set_id": ["b77f9893-a422-423a-bb27-527377ade36d"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-319-30)", "package_ndc": "71205-319-30", "marketing_start_date": "20190901"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-319-60)", "package_ndc": "71205-319-60", "marketing_start_date": "20190901"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-319-90)", "package_ndc": "71205-319-90", "marketing_start_date": "20190901"}], "brand_name": "Tolterodine Tartrate", "product_id": "71205-319_df5371c1-a1d3-4e6d-af7a-17cb46d7653d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "71205-319", "generic_name": "Tolterodine Tartrate", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tolterodine Tartrate", "active_ingredients": [{"name": "TOLTERODINE TARTRATE", "strength": "1 mg/1"}], "application_number": "ANDA077006", "marketing_category": "ANDA", "marketing_start_date": "20151101", "listing_expiration_date": "20261231"}