Flavoxate Hydrochloride
Flavoxate Hydrochloride is listed in the FDA National Drug Code directory with 3 NDC codes, marketed under brand name including Flavoxate Hydrochloride. Available dosage forms: tablet, powder.
Drug Details
- Generic Name
- Flavoxate Hydrochloride
- Brand Names
- Flavoxate Hydrochloride
- Application Number
- ANDA076835
- Sponsor
- PuraCap Laboratories LLC dba Blu Pharmaceuticals
- NDC Codes
- 3
- Dosage Forms
- TABLET, POWDER
- Routes
- ORAL
- Active Ingredients
- FLAVOXATE HYDROCHLORIDE
Indications and Usage
INDICATIONS AND USAGE Flavoxate hydrochloride tablets are indicated for symptomatic relief of dysuria, urgency, nocturia, suprapubic pain, frequency and incontinence as may occur in cystitis, prostatitis, urethritis, urethrocystitis/urethrotrigonitis. Flavoxate hydrochloride tablets are not indicated for definitive treatment, but are compatible with drugs used for the treatment of urinary tract infections.
Warnings
WARNINGS Flavoxate hydrochloride should be given cautiously in patients with suspected glaucoma.