flavoxate hydrochloride

Generic: flavoxate hydrochloride

Labeler: padagis us llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name flavoxate hydrochloride
Generic Name flavoxate hydrochloride
Labeler padagis us llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

flavoxate hydrochloride 100 mg/1

Manufacturer
Padagis US LLC

Identifiers & Regulatory

Product NDC 0574-0115
Product ID 0574-0115_ff1c0ee9-75d2-478a-9152-0753be81ff11
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076831
Marketing Start 2004-12-22
Marketing End 2026-12-31

Pharmacologic Class

Classes
cholinergic muscarinic antagonist [epc] cholinergic muscarinic antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 05740115
Hyphenated Format 0574-0115

Supplemental Identifiers

RxCUI
1095229
UPC
0305740115015
UNII
9C05J6089W

Packaging Origin

Original Packager
true

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 flavoxate hydrochloride (source: ndc)
Generic Name flavoxate hydrochloride (source: ndc)
Application Number ANDA076831 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0574-0115-01)
source: ndc

Packages (1)

0574-0115-01 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0574-0115-01)

Ingredients (1)

flavoxate hydrochloride (100 mg/1)

Linked Drug Pages (1)

FLAVOXATE HYDROCHLORIDE ndc-match (0.9)

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"}