Package 24658-720-01

Brand: flavoxate hydrochloride

Generic: flavoxate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 24658-720-01
Digits Only 2465872001
Product NDC 24658-720
Description

100 TABLET in 1 BOTTLE (24658-720-01)

Marketing

Marketing Status
Marketed Since 2016-12-15
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": "cdb3dd6e-969c-4f0c-888b-a3e1b7062fda", "openfda": {"upc": ["0324658720012"], "unii": ["9C05J6089W"], "rxcui": ["1095229"], "spl_set_id": ["f6a06eda-2480-4c0d-8d1e-9e3e89d3ee88"], "manufacturer_name": ["PuraCap Laboratories LLC dba Blu Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (24658-720-01)", "package_ndc": "24658-720-01", "marketing_start_date": "20161215"}], "brand_name": "Flavoxate Hydrochloride", "product_id": "24658-720_cdb3dd6e-969c-4f0c-888b-a3e1b7062fda", "dosage_form": "TABLET", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "24658-720", "generic_name": "Flavoxate Hydrochloride", "labeler_name": "PuraCap Laboratories LLC dba Blu Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Flavoxate Hydrochloride", "active_ingredients": [{"name": "FLAVOXATE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA076835", "marketing_category": "ANDA", "marketing_start_date": "20161215", "listing_expiration_date": "20261231"}