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Levothyroxine Sodium - 49349-334-20 - (Levothyroxine Sodium)

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Drug Information of Levothyroxine Sodium

Product NDC: 49349-334
Proprietary Name: Levothyroxine Sodium
Non Proprietary Name: Levothyroxine Sodium
Active Ingredient(s): .075    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: 49349-334
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076752
Marketing Category: ANDA
Start Marketing Date: 20110627

Package Information of Levothyroxine Sodium

Package NDC: 49349-334-20
Package Description: 100 TABLET in 1 CANISTER (49349-334-20)

NDC Information of Levothyroxine Sodium

NDC Code 49349-334-20
Proprietary Name Levothyroxine Sodium
Package Description 100 TABLET in 1 CANISTER (49349-334-20)
Product NDC 49349-334
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levothyroxine Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110627
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name LEVOTHYROXINE SODIUM
Strength Number .075
Strength Unit mg/1
Pharmaceutical Classes l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient]

Complete Information of Levothyroxine Sodium


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