Synthroid - 52125-121-02 - (Levothyroxine Sodium)

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Drug Information of Synthroid

Product NDC: 52125-121
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: 52125-121
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021402
Marketing Category: NDA
Start Marketing Date: 20130329

Package Information of Synthroid

Package NDC: 52125-121-02
Package Description: 30 TABLET in 1 BLISTER PACK (52125-121-02)

NDC Information of Synthroid

NDC Code 52125-121-02
Proprietary Name Synthroid
Package Description 30 TABLET in 1 BLISTER PACK (52125-121-02)
Product NDC 52125-121
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levothyroxine Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130329
Marketing Category Name NDA
Labeler Name REMEDYREPACK 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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