Betaxolol Hydrochloride 10702-0014
Product NDC
10702-0014- Manufacturer
- Kvk-Tech, Inc.
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- November 2, 2011
- Listing Expires
- December 31, 2026
- Application
- ANDA078962
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Betaxolol Hydrochloride | 20 mg/1 |
Drug Class
Adrenergic beta-Antagonists [MoA]beta-Adrenergic Blocker [EPC]
Packaging Options(1)
100 TABLET, COATED in 1 BOTTLE (10702-014-01)