betaxolol

Generic: betaxolol

Labeler: puracap laboratories llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name betaxolol
Generic Name betaxolol
Labeler puracap laboratories llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

betaxolol hydrochloride 10 mg/1

Manufacturer
PuraCap Laboratories LLC

Identifiers & Regulatory

Product NDC 24658-700
Product ID 24658-700_7ee988e7-153d-4d55-b4ec-1a8da8f78f1d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075541
Listing Expiration 2026-12-31
Marketing Start 2016-08-22

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 24658700
Hyphenated Format 24658-700

Supplemental Identifiers

RxCUI
1297753 1297757
UPC
0324658701011
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 (source: ndc)
Generic Name betaxolol (source: ndc)
Application Number ANDA075541 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (24658-700-01)
source: ndc

Packages (1)

24658-700-01 100 TABLET, FILM COATED in 1 BOTTLE (24658-700-01)

Ingredients (1)

betaxolol hydrochloride (10 mg/1)

Linked Drug Pages (1)

Betaxolol ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "7ee988e7-153d-4d55-b4ec-1a8da8f78f1d", "openfda": {"upc": ["0324658701011"], "unii": ["6X97D2XT0O"], "rxcui": ["1297753", "1297757"], "spl_set_id": ["e198244d-fda3-4015-8c01-390f3f88e238"], "manufacturer_name": ["PuraCap Laboratories LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (24658-700-01)", "package_ndc": "24658-700-01", "marketing_start_date": "20161215"}], "brand_name": "Betaxolol", "product_id": "24658-700_7ee988e7-153d-4d55-b4ec-1a8da8f78f1d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "24658-700", "generic_name": "Betaxolol", "labeler_name": "PuraCap Laboratories LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Betaxolol", "active_ingredients": [{"name": "BETAXOLOL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA075541", "marketing_category": "ANDA", "marketing_start_date": "20160822", "listing_expiration_date": "20261231"}