FDA
Carteolol Hydrochloride
The FDA lists this product in 3 strengths and forms.
Composition
- Active ingredients
- CARTEOLOL HYDROCHLORIDE 1%
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- CARTEOLOL HYDROCHLORIDE 1% · Solution/dropsThis page
- CARTEOLOL HYDROCHLORIDE 1% · Solution/dropsANDA076097-001 · Discontinued
- CARTEOLOL HYDROCHLORIDE 1% · Solution/dropsANDA075476-001 · Prescription
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application ANDA075546.
Prognia shows this product information for reference and learning. It is not treatment advice and can lag behind the official text. Always check the current product information and local protocols before prescribing.
At a glance
- Brand name
- Carteolol Hydrochloride
- Route
- Eye
- Dosage form
- Solution/drops
- Applicant
- Bausch and Lomb
- Status
- Discontinued
- FDA approval
- 20 Jan 2000
- Application
- ANDA075546-001