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Levothyroxine Sodium - 49349-038-02 - (Levothyroxine Sodium)

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Drug Information of Levothyroxine Sodium

Product NDC: 49349-038
Proprietary Name: Levothyroxine Sodium
Non Proprietary Name: Levothyroxine Sodium
Active Ingredient(s): .125    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: 49349-038
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076752
Marketing Category: ANDA
Start Marketing Date: 20101020

Package Information of Levothyroxine Sodium

Package NDC: 49349-038-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-038-02)

NDC Information of Levothyroxine Sodium

NDC Code 49349-038-02
Proprietary Name Levothyroxine Sodium
Package Description 30 TABLET in 1 BLISTER PACK (49349-038-02)
Product NDC 49349-038
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levothyroxine Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101020
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name LEVOTHYROXINE SODIUM
Strength Number .125
Strength Unit mg/1
Pharmaceutical Classes l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient]

Complete Information of Levothyroxine Sodium


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