Package 0574-0115-01
Brand: flavoxate hydrochloride
Generic: flavoxate hydrochloridePackage Facts
Identity
Package NDC
0574-0115-01
Digits Only
0574011501
Product NDC
0574-0115
Description
100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0574-0115-01)
Marketing
Marketing Status
Brand
flavoxate hydrochloride
Generic
flavoxate hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ff1c0ee9-75d2-478a-9152-0753be81ff11", "openfda": {"upc": ["0305740115015"], "unii": ["9C05J6089W"], "rxcui": ["1095229"], "spl_set_id": ["a9c44c4b-5b3c-45bf-9bc9-ce858e3d06c5"], "manufacturer_name": ["Padagis US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0574-0115-01)", "package_ndc": "0574-0115-01", "marketing_end_date": "20261231", "marketing_start_date": "20041222"}], "brand_name": "FLAVOXATE HYDROCHLORIDE", "product_id": "0574-0115_ff1c0ee9-75d2-478a-9152-0753be81ff11", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "0574-0115", "generic_name": "FLAVOXATE HYDROCHLORIDE", "labeler_name": "Padagis US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FLAVOXATE HYDROCHLORIDE", "active_ingredients": [{"name": "FLAVOXATE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA076831", "marketing_category": "ANDA", "marketing_end_date": "20261231", "marketing_start_date": "20041222"}