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Levothyroxine sodium - 35356-933-30 - (Levothyroxine sodium)

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Drug Information of Levothyroxine sodium

Product NDC: 35356-933
Proprietary Name: Levothyroxine sodium
Non Proprietary Name: Levothyroxine sodium
Active Ingredient(s): 25    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: 35356-933
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021342
Marketing Category: NDA
Start Marketing Date: 20020301

Package Information of Levothyroxine sodium

Package NDC: 35356-933-30
Package Description: 30 TABLET in 1 BOTTLE (35356-933-30)

NDC Information of Levothyroxine sodium

NDC Code 35356-933-30
Proprietary Name Levothyroxine sodium
Package Description 30 TABLET in 1 BOTTLE (35356-933-30)
Product NDC 35356-933
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 Lake Erie Medical DBA Quality Care Products LLC
Substance Name LEVOTHYROXINE SODIUM
Strength Number 25
Strength Unit ug/1
Pharmaceutical Classes l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient]

Complete Information of Levothyroxine sodium


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