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Levothyroxine sodium - Medication Information

Product NDC Code 70771-1819
Drug Name

Levothyroxine sodium

Type Generic
Pharm Class Thyroxine [CS],
l-Thyroxine [EPC]
Active Ingredients
Levothyroxine sodium anhydrous 500 ug/5ml
Route INTRAVENOUS
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
RxCUI drug identifier 1115267
Application Number ANDA217066
Labeler Name Zydus Lifesciences Limited
Packages
Package NDC Code Description
70771-1819-1 1 vial, single-dose in 1 carton (70771-1819-1) / 5 ml in 1 vial, single-dose
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Spl product data elements

Usually a list of ingredients in a drug product.
LEVOTHYROXINE SODIUM levothyroxine sodium LEVOTHYROXINE SODIUM ANHYDROUS LEVOTHYROXINE MANNITOL SODIUM HYDROXIDE white to off-white LEVOTHYROXINE SODIUM levothyroxine sodium LEVOTHYROXINE SODIUM ANHYDROUS LEVOTHYROXINE MANNITOL SODIUM HYDROXIDE white to off-white LEVOTHYROXINE SODIUM levothyroxine sodium LEVOTHYROXINE SODIUM ANHYDROUS LEVOTHYROXINE MANNITOL SODIUM HYDROXIDE white to off-white

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 70771-1818-1 Levothyroxine Sodium for Injection 100 mcg per vial For Intravenous Use Discard any unused portion Single-Dose Vial Rx only NDC 70771-1819-1 Levothyroxine Sodium for Injection 200 mcg per vial For Intravenous Use Discard any unused portion Single-Dose Vial Rx only NDC 70771-1820-1 Levothyroxine Sodium for Injection 500 mcg per vial For Intravenous Use Discard any unused portion Single-Dose Vial Rx only 100 mcg carton label 200 mcg carton label 500 mcg label

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