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Levothyroxine Sodium - 0378-1817-10 - (levothyroxine sodium)

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Drug Information of Levothyroxine Sodium

Product NDC: 0378-1817
Proprietary Name: Levothyroxine Sodium
Non Proprietary Name: levothyroxine sodium
Active Ingredient(s): 175    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: 0378-1817
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076187
Marketing Category: ANDA
Start Marketing Date: 20120808

Package Information of Levothyroxine Sodium

Package NDC: 0378-1817-10
Package Description: 1000 TABLET in 1 BOTTLE, PLASTIC (0378-1817-10)

NDC Information of Levothyroxine Sodium

NDC Code 0378-1817-10
Proprietary Name Levothyroxine Sodium
Package Description 1000 TABLET in 1 BOTTLE, PLASTIC (0378-1817-10)
Product NDC 0378-1817
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name levothyroxine sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120808
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
Substance Name LEVOTHYROXINE SODIUM
Strength Number 175
Strength Unit ug/1
Pharmaceutical Classes l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient]

Complete Information of Levothyroxine Sodium


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