United States· US:42806-058_6aeb8856-3df7-40a7-b03e-d855a58c8fa4
Flavoxate Hydrochloride
A flavoxate product containing flavoxate hydrochloride, registered in United States by Epic Pharma, LLC. The same ATC class is registered in 7 of our 19 countries.
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
Where it is registered
Flavoxate is registered in 7 of 19 countries.
Countries holding a registration under ATC G04BD02 (flavoxate), each read from that country’s own register.
- This record: United States, from FDA National Drug Code directory (United States)
- 3 of them publish a price we can compare per daily dose
Flavoxate · ATC G04BD02
7 / 19 countries
- Belgiumprice
- Germany
- Ireland
- Netherlands
- Switzerlandprice
- United Kingdom
- United Statesprice
Price per daily dose
What a daily dose of flavoxate costs, country by country.
Normalised to the WHO defined daily dose (0.8 g), so markets compare like for like.
- 1 market with a comparable price for this class
- Public list prices, converted to USD at the rate date shown
Flavoxate · price per daily dose (0.8 g)
USD · FX 28 Sept 2026
- CH Switzerland$2.26
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- FLAVOXATE HYDROCHLORIDE
- Manufacturer
- Epic Pharma, LLC
- Country
- United States (US)
- ATC code
- G04BD02
- ATC class
- Flavoxate
- Defined daily dose
- 0.8 g, O
- Reimbursed
- Not published by this register
- Source register
- FDA National Drug Code directory (United States)
- Last checked
- September 27, 2026
Packs & prices · 4
- ndc114280605801100 TABLET in 1 BOTTLE (42806-058-01)
- ndc1142806058101000 TABLET in 1 BOTTLE (42806-058-10)
- ndc1142806-058-01
- ndc1142806-058-10
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
132 interactions on record for flavoxate.
Graded by severity as the source publishes them — 3 severe. Severity grades are free for everyone; mechanism and management come with Growth.
- Severity for every pair — free, no plan needed
- The source, licence and sync date on every record
- Mechanism and what to do for each pair — Growth plan
Flavoxate · interactions on record
132 records
- 3 severe
- 89 moderate
- 1 minor
Most severe, free to view
- Potassium chlorideA12BA01severe
- Potassium citrateA12BA02severe
- Potassium chlorideB05XA01severe
- DicycloverineA03AA07moderate
39 more interactions with mechanism and management, from a commercially licensed source.
Sign in to check- Interaction severity from DDInter 2.0 (Xiong G. et al., Nucleic Acids Res.), licensed CC BY-NC 4.0 — free for non-commercial use only; not covered by the Drug Database commercial licence.
Same medicine, other countries
Flavoxate in 8 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United KingdomFlavoxate 100mg/5ml oral solutionSpecial Order
- SwitzerlandUrispas, FilmtablettenRECORDATI AG
- BelgiumUrispas 200 mgRecordati Ireland
- IrelandUrispas 200 mg Film-coated TabletsRecordati Ireland Limited
- NetherlandsUrispas, omhulde tabletten 200 mgRecordati Ireland Ltd. (Co. Cork)
- FranceURISPAS 200 mg, comprimé pelliculéBOUCHARA-RECORDATI
- GermanySpasuret 200 MgRecordati Pharma Gmbh
- SpainURONID 200 MG COMPRIMIDOS RECUBIERTOS CON PELÍCULACasen Recordati S.L.
Authorised across Europe · EMA
The same active substance is authorised in 11 EEA countries. Names it is sold under:
- Belgium · Urispas
- Germany · Spasuret 200 Mg
- Spain · Uronid
- France · Urispas
- United Kingdom (Northern Ireland) · Urispas
- Ireland · Urispas
- Italy · Genurin
- Lithuania · Urispas
- Luxembourg · Urispas
- Netherlands · Urispas
- Portugal · Urispás
Source: European Medicines Agency, Article 57 product data.
Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of FDA National Drug Code directory (United States). This is an informational data service and not a medical device — verify against the official source of record before any clinical decision.
For developers
The same record over the API, and the raw payload
GET /v1/drugs/e9f6ac09-33dd-45b3-9dcc-33e62b929e70 GET /v1/drugs/e9f6ac09-33dd-45b3-9dcc-33e62b929e70?format=fhir
Every response carries last_synced_at, so freshness is a field rather than a promise. Below is exactly what the ingestion wrote, before any presentation — the same JSON the API returns under payload.
{
"route": "ORAL",
"source": "ndc",
"strength": "100",
"substance": "FLAVOXATE HYDROCHLORIDE",
"productndc": "42806-058",
"dosage_form": "TABLET",
"dea_schedule": null,
"strength_unit": "mg/1",
"application_number": "ANDA076835",
"marketing_category": "ANDA"
}See everything about flavoxate.
This page is the registration. A free account adds the label text as the regulator wrote it, what it costs per daily dose across the markets that publish a price, a feed of what changes in the registers, and an assistant that answers with its sources. Interaction severity is free; mechanism and management are on the Growth plan. No card, nothing to install.