NDC 0093-4235

Nadolol

Nadolol

Nadolol is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Teva Pharmaceuticals Usa, Inc.. The primary component is Nadolol.

Product ID0093-4235_af5152c5-3641-4622-9295-02e9ac51b0d5
NDC0093-4235
Product TypeHuman Prescription Drug
Proprietary NameNadolol
Generic NameNadolol
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2008-11-03
Marketing CategoryANDA / ANDA
Application NumberANDA074229
Labeler NameTeva Pharmaceuticals USA, Inc.
Substance NameNADOLOL
Active Ingredient Strength20 mg/1
Pharm ClassesAdrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 0093-4235-01

100 TABLET in 1 BOTTLE (0093-4235-01)
Marketing Start Date2008-11-03
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0093-4235-01 [00093423501]

Nadolol TABLET
Marketing CategoryANDA
Application NumberANDA074229
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2008-11-03

Drug Details

Active Ingredients

IngredientStrength
NADOLOL20 mg/1

OpenFDA Data

SPL SET ID:0031ce9c-cb49-433a-aa74-8d20ca0563c0
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 198006
  • 198007
  • 198008
  • UPC Code
  • 0300934236019
  • 0300934235012
  • Pharmacological Class

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

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

    NDCBrand NameGeneric Name
    0093-4235NadololNadolol
    0093-4236NadololNadolol
    0093-4237NadololNadolol
    0378-0028Nadololnadolol
    0378-1132Nadololnadolol
    0378-1171Nadololnadolol
    0781-1181NadololNadolol
    0781-1182NadololNadolol
    0781-1183NadololNadolol
    0781-8004NadololNadolol
    0781-8005NadololNadolol
    0781-8006NadololNadolol
    0904-7070NadololNadolol
    0904-7071NadololNadolol
    10135-686NadololNadolol
    10135-687NadololNadolol
    10135-688NadololNadolol
    21695-799NadololNadolol
    21695-800NadololNadolol
    21695-802NadololNadolol
    23155-730NadololNadolol
    23155-731NadololNadolol
    23155-732NadololNadolol
    67787-349NadololNadolol
    67787-347NadololNadolol
    67787-348NadololNadolol
    68001-317NadololNadolol
    68001-319NadololNadolol
    68001-318NadololNadolol
    68258-6034NadololNadolol
    68382-734NadololNadolol
    68382-732NadololNadolol
    68382-733NadololNadolol
    69097-869NadololNadolol
    69238-1123NadololNadolol
    69097-867NadololNadolol
    69097-868NadololNadolol
    69238-1124NadololNadolol
    69238-1125NadololNadolol
    70518-1755NadololNadolol
    70771-1090NadololNadolol
    70771-1091NadololNadolol
    70771-1089NadololNadolol
    71335-0697NadololNadolol
    31722-349NadololNadolol
    31722-347NadololNadolol
    31722-348NadololNadolol
    42254-218NadololNadolol
    42254-094NadololNadolol
    50742-180NADOLOLNADOLOL

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.