Package 0904-6593-04

Brand: tolterodine tartrate

Generic: tolterodine
NDC Package

Package Facts

Identity

Package NDC 0904-6593-04
Digits Only 0904659304
Product NDC 0904-6593
Description

30 BLISTER PACK in 1 CARTON (0904-6593-04) / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK

Marketing

Marketing Status
Discontinued 2026-07-31
Brand tolterodine tartrate
Generic tolterodine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "15347509-36ce-4dfc-91e3-9e41f06aa50a", "openfda": {"unii": ["5T619TQR3R"], "rxcui": ["855182", "855189"], "spl_set_id": ["da9423b5-00ab-46fc-8959-3db3c0a0bc6d"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (0904-6593-04)  / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "0904-6593-04", "marketing_end_date": "20260731", "marketing_start_date": "20150811"}], "brand_name": "TOLTERODINE TARTRATE", "product_id": "0904-6593_15347509-36ce-4dfc-91e3-9e41f06aa50a", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "0904-6593", "generic_name": "TOLTERODINE", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TOLTERODINE TARTRATE", "active_ingredients": [{"name": "TOLTERODINE TARTRATE", "strength": "4 mg/1"}], "application_number": "ANDA203016", "marketing_category": "ANDA", "marketing_end_date": "20260731", "marketing_start_date": "20150811"}