Betaxolol
- Strength
- 20 mg/1
- Form
- Tablet, Film Coated
- Class
- beta-Adrenergic Blocker
Epic Pharma LLC
betaxolol hydrochloride
Listed by Novartis Pharmaceuticals Corporation
| Dosage form | Suspension/ Drops |
|---|---|
| Route | Ophthalmic |
| Drug class | beta-Adrenergic Blocker |
| Approval route | NDA — original brand approval |
| NDC code | 0078-0729 |
| FDA application | NDA019845 |
| RxNorm concept | 213729 |
| Package sizes listed | 2 |
| Marketed since | January 1996 |
Same active ingredient, different manufacturer, strength or form. Products matching on both ingredient and strength are usually interchangeable — but confirm before switching, especially with modified-release forms.
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Information only, not medical advice. Nothing on this page indicates that a medication is safe or suitable for you. Speak to a prescriber or pharmacist before starting, stopping or switching any medicine.
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