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Levothyroxine Sodium - 54868-2131-0 - (levothyroxine sodium)

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Drug Information of Levothyroxine Sodium

Product NDC: 54868-2131
Proprietary Name: Levothyroxine Sodium
Non Proprietary Name: levothyroxine sodium
Active Ingredient(s): 50    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: 54868-2131
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076187
Marketing Category: ANDA
Start Marketing Date: 20050309

Package Information of Levothyroxine Sodium

Package NDC: 54868-2131-0
Package Description: 30 TABLET in 1 BOTTLE (54868-2131-0)

NDC Information of Levothyroxine Sodium

NDC Code 54868-2131-0
Proprietary Name Levothyroxine Sodium
Package Description 30 TABLET in 1 BOTTLE (54868-2131-0)
Product NDC 54868-2131
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name levothyroxine sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20050309
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name LEVOTHYROXINE SODIUM
Strength Number 50
Strength Unit ug/1
Pharmaceutical Classes l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient]

Complete Information of Levothyroxine Sodium


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