Package 58151-099-91

Brand: detrol

Generic: tolterodine tartrate
NDC Package

Package Facts

Identity

Package NDC 58151-099-91
Digits Only 5815109991
Product NDC 58151-099
Description

60 TABLET, FILM COATED in 1 BOTTLE (58151-099-91)

Marketing

Marketing Status
Discontinued 2027-01-31
Brand detrol
Generic tolterodine tartrate
Sample Package No

Linked Drug Pages (1)

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 (58151-099-91)", "package_ndc": "58151-099-91", "marketing_end_date": "20270131", "marketing_start_date": "20240801"}], "brand_name": "Detrol", "product_id": "58151-099_f27726af-7a9b-45f4-96e0-1e90a5fdcc18", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "58151-099", "generic_name": "tolterodine tartrate", "labeler_name": "Viatris Specialty LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Detrol", "active_ingredients": [{"name": "TOLTERODINE TARTRATE", "strength": "2 mg/1"}], "application_number": "NDA020771", "marketing_category": "NDA", "marketing_end_date": "20270131", "marketing_start_date": "20240801"}