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Levothyroxine Sodium - 49349-639-02 - (Levothyroxine Sodium)

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Drug Information of Levothyroxine Sodium

Product NDC: 49349-639
Proprietary Name: Levothyroxine Sodium
Non Proprietary Name: Levothyroxine Sodium
Active Ingredient(s): .137    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: 49349-639
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021210
Marketing Category: NDA
Start Marketing Date: 20111208

Package Information of Levothyroxine Sodium

Package NDC: 49349-639-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-639-02)

NDC Information of Levothyroxine Sodium

NDC Code 49349-639-02
Proprietary Name Levothyroxine Sodium
Package Description 30 TABLET in 1 BLISTER PACK (49349-639-02)
Product NDC 49349-639
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levothyroxine Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111208
Marketing Category Name NDA
Labeler Name REMEDYREPACK INC.
Substance Name LEVOTHYROXINE SODIUM
Strength Number .137
Strength Unit mg/1
Pharmaceutical Classes l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient]

Complete Information of Levothyroxine Sodium


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