Synthroid - 68258-5972-9 - (Levothyroxine Sodium)

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Drug Information of Synthroid

Product NDC: 68258-5972
Proprietary Name: Synthroid
Non Proprietary Name: Levothyroxine Sodium
Active Ingredient(s): 88    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: 68258-5972
Labeler Name: Dispensing Solutions, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021402
Marketing Category: NDA
Start Marketing Date: 20020724

Package Information of Synthroid

Package NDC: 68258-5972-9
Package Description: 90 TABLET in 1 BOTTLE (68258-5972-9)

NDC Information of Synthroid

NDC Code 68258-5972-9
Proprietary Name Synthroid
Package Description 90 TABLET in 1 BOTTLE (68258-5972-9)
Product NDC 68258-5972
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levothyroxine Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20020724
Marketing Category Name NDA
Labeler Name Dispensing Solutions, Inc.
Substance Name LEVOTHYROXINE SODIUM
Strength Number 88
Strength Unit ug/1
Pharmaceutical Classes l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient]

Complete Information of Synthroid


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