NDC 24658-700
Betaxolol
Betaxolol
Betaxolol is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Puracap Laboratories Llc. The primary component is Betaxolol Hydrochloride.
Product ID | 24658-700_7ee988e7-153d-4d55-b4ec-1a8da8f78f1d |
NDC | 24658-700 |
Product Type | Human Prescription Drug |
Proprietary Name | Betaxolol |
Generic Name | Betaxolol |
Dosage Form | Tablet, Film Coated |
Route of Administration | ORAL |
Marketing Start Date | 2016-08-22 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA075541 |
Labeler Name | PuraCap Laboratories LLC |
Substance Name | BETAXOLOL HYDROCHLORIDE |
Active Ingredient Strength | 10 mg/1 |
Pharm Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |