Betaxolol 24658-0700
Product NDC
24658-0700- Manufacturer
- Puracap Laboratories Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 22, 2016
- Listing Expires
- December 31, 2026
- Application
- ANDA075541
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Betaxolol Hydrochloride | 10 mg/1 |
Drug Class
Adrenergic beta-Antagonists [MoA]beta-Adrenergic Blocker [EPC]
Packaging Options(1)
100 TABLET, FILM COATED in 1 BOTTLE (24658-700-01)