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Levothyroxine sodium - 0781-5187-01 - (Levothyroxine sodium)

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Drug Information of Levothyroxine sodium

Product NDC: 0781-5187
Proprietary Name: Levothyroxine sodium
Non Proprietary Name: Levothyroxine sodium
Active Ingredient(s): 150    ug/1 & nbsp;   Levothyroxine sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Levothyroxine sodium

Product NDC: 0781-5187
Labeler Name: Sandoz Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021342
Marketing Category: NDA
Start Marketing Date: 20020301

Package Information of Levothyroxine sodium

Package NDC: 0781-5187-01
Package Description: 100 TABLET in 1 BOTTLE (0781-5187-01)

NDC Information of Levothyroxine sodium

NDC Code 0781-5187-01
Proprietary Name Levothyroxine sodium
Package Description 100 TABLET in 1 BOTTLE (0781-5187-01)
Product NDC 0781-5187
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levothyroxine sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20020301
Marketing Category Name NDA
Labeler Name Sandoz Inc.
Substance Name LEVOTHYROXINE SODIUM
Strength Number 150
Strength Unit ug/1
Pharmaceutical Classes l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient]

Complete Information of Levothyroxine sodium


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