FDA
Levobunolol Hydrochloride
The FDA lists this product in 6 strengths and forms.
Composition
- Active ingredients
- LEVOBUNOLOL HYDROCHLORIDE 0.25%
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- LEVOBUNOLOL HYDROCHLORIDE 0.5% · Solution/dropsANDA075475-001 · Discontinued
- LEVOBUNOLOL HYDROCHLORIDE 0.25% · Solution/dropsANDA075473-001 · Discontinued
- LEVOBUNOLOL HYDROCHLORIDE 0.5% · Solution/dropsANDA074850-001 · Discontinued
- LEVOBUNOLOL HYDROCHLORIDE 0.25% · Solution/dropsANDA074851-001 · Discontinued
- LEVOBUNOLOL HYDROCHLORIDE 0.5% · Solution/dropsANDA074326-001 · Prescription
- LEVOBUNOLOL HYDROCHLORIDE 0.25% · Solution/dropsThis page
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application ANDA074307.
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
- Levobunolol Hydrochloride
- Route
- Eye
- Dosage form
- Solution/drops
- Applicant
- Bausch and Lomb
- Status
- Discontinued
- FDA approval
- 4 Mar 1994
- Application
- ANDA074307-001