NDC 10702-014 – Betaxolol Hydrochloride
Betaxolol Hydrochloride 20 mg/1 · Tablet, Coated · Oral
Product NDC10702-014
Product details
- Brand name
- Betaxolol Hydrochloride
- Generic name
- Betaxolol hydrochloride
- Labeler
- KVK-TECH, INC.
- Dosage form
- Tablet, Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078962
- Marketed since
- November 2, 2011
- Listing expires
- December 31, 2026
- Pharmacologic class
- beta-Adrenergic Blocker
Active ingredients
- Betaxolol Hydrochloride 20 mg/1
Uses, dosage, side effects and warnings for Betaxolol Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 10702-014-01 | 100 TABLET, COATED in 1 BOTTLE (10702-014-01) | Nov 2, 2011 |
Recalls mentioning this NDC
- D-0049-2024 Oct 25, 2023 · Class I
Presence of Foreign Tablets/Capsules: There is a potential presence of oxycodone HCl tablets, USP 5 mg in bottles.