Home
>
National Drug Code (NDC)
>
BETAXOLOL HYDROCHLORIDE
BETAXOLOL HYDROCHLORIDE - 10702-014-01 - (betaxolol hydrochloride)
Drug Information of BETAXOLOL HYDROCHLORIDE
| Product NDC: | 10702-014 |
| Proprietary Name: | BETAXOLOL HYDROCHLORIDE |
| Non Proprietary Name: | betaxolol hydrochloride |
| Active Ingredient(s): | 20 mg/1 & nbsp; betaxolol hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BETAXOLOL HYDROCHLORIDE
| Product NDC: | 10702-014 |
| Labeler Name: | KVK-TECH, INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078962 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111102 |
Package Information of BETAXOLOL HYDROCHLORIDE
| Package NDC: | 10702-014-01 |
| Package Description: | 100 TABLET, COATED in 1 BOTTLE (10702-014-01) |
NDC Information of BETAXOLOL HYDROCHLORIDE
| NDC Code | 10702-014-01 |
| Proprietary Name | BETAXOLOL HYDROCHLORIDE |
| Package Description | 100 TABLET, COATED in 1 BOTTLE (10702-014-01) |
| Product NDC | 10702-014 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | betaxolol hydrochloride |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20111102 |
| Marketing Category Name | ANDA |
| Labeler Name | KVK-TECH, INC. |
| Substance Name | BETAXOLOL HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
