NDC 24658-701

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 ID24658-701_7ee988e7-153d-4d55-b4ec-1a8da8f78f1d
NDC24658-701
Product TypeHuman Prescription Drug
Proprietary NameBetaxolol
Generic NameBetaxolol
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2016-08-22
Marketing CategoryANDA / ANDA
Application NumberANDA075541
Labeler NamePuraCap Laboratories LLC
Substance NameBETAXOLOL HYDROCHLORIDE
Active Ingredient Strength20 mg/1
Pharm ClassesAdrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 24658-701-01

100 TABLET, FILM COATED in 1 BOTTLE (24658-701-01)
Marketing Start Date2016-12-15
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 24658-701-01 [24658070101]

Betaxolol TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075541
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2016-12-15

Drug Details

Active Ingredients

IngredientStrength
BETAXOLOL HYDROCHLORIDE20 mg/1

OpenFDA Data

SPL SET ID:e198244d-fda3-4015-8c01-390f3f88e238
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1297757
  • 1297753
    • UPC Code
  • 0324658701011

    • Pharmacological Class

    • Adrenergic beta-Antagonists [MoA]
    • beta-Adrenergic Blocker [EPC]

    NDC Crossover Matching brand name "Betaxolol" or generic name "Betaxolol"

    NDCBrand NameGeneric Name
    10135-623BetaxololBetaxolol
    10135-624BetaxololBetaxolol
    17478-705BetaxololBetaxolol Hydrochloride
    24658-700BetaxololBetaxolol
    24658-701BetaxololBetaxolol
    42806-038BetaxololBetaxolol
    42806-039BetaxololBetaxolol
    60429-753BetaxololBetaxolol
    60429-754BetaxololBetaxolol
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