Composition
- Active ingredients
- BENOXINATE HYDROCHLORIDE 0.4%
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application ANDA084149.
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
- Benoxinate Hydrochloride
- Route
- Eye
- Dosage form
- Solution/drops
- Applicant
- Sola Barnes Hind
- Status
- Discontinued
- FDA approval
- 14 Jan 1975
- Application
- ANDA084149-001