betaxolol hydrochloride

Generic: betaxolol hydrochloride

Labeler: kvk-tech, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name betaxolol hydrochloride
Generic Name betaxolol hydrochloride
Labeler kvk-tech, inc.
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

betaxolol hydrochloride 20 mg/1

Manufacturer
KVK-TECH, INC.

Identifiers & Regulatory

Product NDC 10702-014
Product ID 10702-014_1757ca78-c783-c977-e063-6294a90a7862
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078962
Listing Expiration 2026-12-31
Marketing Start 2011-11-02

Pharmacologic Class

Classes
adrenergic beta-antagonists [moa] beta-adrenergic blocker [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 10702014
Hyphenated Format 10702-014

Supplemental Identifiers

RxCUI
1297753 1297757
UNII
6X97D2XT0O

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name betaxolol hydrochloride (source: ndc)
Generic Name betaxolol hydrochloride (source: ndc)
Application Number ANDA078962 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET, COATED in 1 BOTTLE (10702-014-01)
source: ndc

Packages (1)

10702-014-01 100 TABLET, COATED in 1 BOTTLE (10702-014-01)

Ingredients (1)

betaxolol hydrochloride (20 mg/1)

Linked Drug Pages (1)

BETAXOLOL HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1757ca78-c783-c977-e063-6294a90a7862", "openfda": {"unii": ["6X97D2XT0O"], "rxcui": ["1297753", "1297757"], "spl_set_id": ["f3b50bbb-df03-4ed7-9d8d-180edc2abd54"], "manufacturer_name": ["KVK-TECH, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (10702-014-01)", "package_ndc": "10702-014-01", "marketing_start_date": "20111102"}], "brand_name": "BETAXOLOL HYDROCHLORIDE", "product_id": "10702-014_1757ca78-c783-c977-e063-6294a90a7862", "dosage_form": "TABLET, COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "10702-014", "generic_name": "betaxolol hydrochloride", "labeler_name": "KVK-TECH, INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BETAXOLOL HYDROCHLORIDE", "active_ingredients": [{"name": "BETAXOLOL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA078962", "marketing_category": "ANDA", "marketing_start_date": "20111102", "listing_expiration_date": "20261231"}