Composition
- Active ingredients
- BETHANECHOL CHLORIDE 50MG
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- BETHANECHOL CHLORIDE 10MG · TabletANDA088440-001 · Discontinued
- BETHANECHOL CHLORIDE 25MG · TabletANDA088441-001 · Discontinued
- BETHANECHOL CHLORIDE 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · TabletNDA006536-004 · Discontinued
- BETHANECHOL CHLORIDE 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · TabletNDA006536-002 · Discontinued
- BETHANECHOL CHLORIDE 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · TabletNDA006536-005 · Discontinued
- BETHANECHOL CHLORIDE 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · TabletNDA006536-003 · Discontinued
- BETHANECHOL CHLORIDE 5MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · InjectableNDA006536-001 · Discontinued
- BETHANECHOL CHLORIDE 5MG · TabletANDA089095-001 · Discontinued
- BETHANECHOL CHLORIDE 50MG · TabletThis page
At a glance
- Brand name
- Urecholine
- Active substance
- bethanechol chloride
- Route
- Oral
- Dosage form
- Tablet
- Applicant
- Odyssey Pharms
- Status
- Discontinued
- FDA approval
- 19 Dec 1985
- Application
- ANDA089096-001