Flavoxate Hydrochloride
Active substance: flavoxate
TABLET · FLAVOXATE HYDROCHLORIDE 100 mg/1
United StatesActive
Marketing holder: PuraCap Laboratories LLC dba Blu Pharmaceuticals
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
Composition
- FLAVOXATE HYDROCHLORIDE · 100 mg/1
Import and control
Control by country
- United Statesprescription only
Source: openFDA NDC · record 01a12091-755c-7879-b125-135755d5a9f8,01a12093-6a29-7145-8f83-cbaa733e6052,01a1209e-77cf-730b-8492-ec2bcaa39296;count=3 · valid from 2026-10-09 · verified 2026-10-09
Registration
- Registration number
- 24658-720
- Registration status
- Active
- Dispensing
- Prescription only
- Route
- ORAL
Sources
- product · openFDA NDC · 24658-720 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 24658-720 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 24658-720 · Verified 2026-10-09 · open in source