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FDA Drug information

Nadolol

Read time: 1 mins
Marketing start date: 28 Apr 2024

Summary of product characteristics


Effective Time

20221031

Version

4

Spl Product Data Elements

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

Application Number

ANDA207761

Brand Name

Nadolol

Generic Name

Nadolol

Product Ndc

70771-1089

Product Type

HUMAN PRESCRIPTION DRUG

Route

ORAL

Package Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL NDC 70771-1089-9 Nadolol tablets, 20 mg Rx only 90 tablets NDC 70771-1090-9 Nadolol tablets, 40 mg Rx only 90 tablets NDC 70771-1091-9 Nadolol tablets, 80 mg Rx only 80 tablets Nadolol tablets Nadolol tablets Nadolol tablets

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