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Nadolol - Medication Information

Product NDC Code 70771-1089
Drug Name

Nadolol

Type Generic
Pharm Class Adrenergic beta-Antagonists [MoA],
beta-Adrenergic Blocker [EPC]
Active Ingredients
Nadolol 20 mg/1
Route ORAL
Dosage Form TABLET
RxCUI drug identifier 198006,
198007,
198008
Application Number ANDA207761
Labeler Name Zydus Lifesciences Limited
Packages
Package NDC Code Description
70771-1089-0 1000 tablet in 1 bottle (70771-1089-0)
70771-1089-1 100 tablet in 1 bottle (70771-1089-1)
70771-1089-4 10 blister pack in 1 carton (70771-1089-4) / 1 tablet in 1 blister pack (70771-1089-2)
70771-1089-9 90 tablet in 1 bottle (70771-1089-9)
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Spl product data elements

Usually a list of ingredients in a drug product.
Nadolol Nadolol NADOLOL NADOLOL ANHYDROUS CITRIC ACID CELLULOSE, MICROCRYSTALLINE FERRIC OXIDE YELLOW MAGNESIUM STEARATE POVIDONE SILICON DIOXIDE SODIUM STARCH GLYCOLATE TYPE A POTATO STARCH, CORN YELLOW ROUND N;40 Nadolol Nadolol NADOLOL NADOLOL ANHYDROUS CITRIC ACID CELLULOSE, MICROCRYSTALLINE FD&C BLUE NO. 2 MAGNESIUM STEARATE POVIDONE SILICON DIOXIDE SODIUM STARCH GLYCOLATE TYPE A POTATO STARCH, CORN BLUE ROUND N;80 Nadolol Nadolol NADOLOL NADOLOL ANHYDROUS CITRIC ACID CELLULOSE, MICROCRYSTALLINE MAGNESIUM STEARATE POVIDONE SILICON DIOXIDE SODIUM STARCH GLYCOLATE TYPE A POTATO STARCH, CORN OFF-WHITE ROUND N;20

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL NDC 70771-1089-1 Nadolol tablets, 20 mg Rx only 100 tablets NDC 70771-1090-1 Nadolol tablets, 40 mg Rx only 100 tablets NDC 70771-1091-1 Nadolol tablets, 80 mg Rx only 100 tablets Nadolol tablets Nadolol tablets Nadolol tablets

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API