flavoxate hydrochloride

Generic: flavoxate hydrochloride

Labeler: epic pharma, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name flavoxate hydrochloride
Generic Name flavoxate hydrochloride
Labeler epic pharma, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

flavoxate hydrochloride 100 mg/1

Manufacturer
Epic Pharma, LLC

Identifiers & Regulatory

Product NDC 42806-058
Product ID 42806-058_6aeb8856-3df7-40a7-b03e-d855a58c8fa4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076835
Listing Expiration 2026-12-31
Marketing Start 2011-02-21

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42806058
Hyphenated Format 42806-058

Supplemental Identifiers

RxCUI
1095229
UPC
0342806058015
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 ANDA076835 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (42806-058-01)
  • 1000 TABLET in 1 BOTTLE (42806-058-10)
source: ndc

Packages (2)

42806-058-01 100 TABLET in 1 BOTTLE (42806-058-01) 42806-058-10 1000 TABLET in 1 BOTTLE (42806-058-10)

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": "6aeb8856-3df7-40a7-b03e-d855a58c8fa4", "openfda": {"upc": ["0342806058015"], "unii": ["9C05J6089W"], "rxcui": ["1095229"], "spl_set_id": ["b4260d7e-2ab3-49f6-aa57-bae19a23d82a"], "manufacturer_name": ["Epic Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (42806-058-01)", "package_ndc": "42806-058-01", "marketing_start_date": "20110221"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (42806-058-10)", "package_ndc": "42806-058-10", "marketing_start_date": "20110221"}], "brand_name": "Flavoxate Hydrochloride", "product_id": "42806-058_6aeb8856-3df7-40a7-b03e-d855a58c8fa4", "dosage_form": "TABLET", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "42806-058", "generic_name": "Flavoxate Hydrochloride", "labeler_name": "Epic Pharma, LLC", "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": "20110221", "listing_expiration_date": "20261231"}