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LEVOTHYROXINE SODIUM - 54868-4507-0 - (Levothyroxine Sodium)

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Drug Information of LEVOTHYROXINE SODIUM

Product NDC: 54868-4507
Proprietary Name: LEVOTHYROXINE SODIUM
Non Proprietary Name: Levothyroxine Sodium
Active Ingredient(s): .175    mg/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: 54868-4507
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076187
Marketing Category: ANDA
Start Marketing Date: 20010416

Package Information of LEVOTHYROXINE SODIUM

Package NDC: 54868-4507-0
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (54868-4507-0)

NDC Information of LEVOTHYROXINE SODIUM

NDC Code 54868-4507-0
Proprietary Name LEVOTHYROXINE SODIUM
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (54868-4507-0)
Product NDC 54868-4507
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levothyroxine Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20010416
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name LEVOTHYROXINE SODIUM
Strength Number .175
Strength Unit mg/1
Pharmaceutical Classes l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient]

Complete Information of LEVOTHYROXINE SODIUM


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