Synthroid - 54868-1011-2 - (Levothyroxine Sodium)

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Drug Information of Synthroid

Product NDC: 54868-1011
Proprietary Name: Synthroid
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 Synthroid

Product NDC: 54868-1011
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021402
Marketing Category: NDA
Start Marketing Date: 20090714

Package Information of Synthroid

Package NDC: 54868-1011-2
Package Description: 30 TABLET in 1 BOTTLE (54868-1011-2)

NDC Information of Synthroid

NDC Code 54868-1011-2
Proprietary Name Synthroid
Package Description 30 TABLET in 1 BOTTLE (54868-1011-2)
Product NDC 54868-1011
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levothyroxine Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090714
Marketing Category Name NDA
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 Synthroid


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