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Levothyroxine Sodium - 49349-859-19 - (Levothyroxine Sodium)

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Drug Information of Levothyroxine Sodium

Product NDC: 49349-859
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: 49349-859
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021342
Marketing Category: NDA
Start Marketing Date: 20111228

Package Information of Levothyroxine Sodium

Package NDC: 49349-859-19
Package Description: 90 TABLET in 1 CANISTER (49349-859-19)

NDC Information of Levothyroxine Sodium

NDC Code 49349-859-19
Proprietary Name Levothyroxine Sodium
Package Description 90 TABLET in 1 CANISTER (49349-859-19)
Product NDC 49349-859
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levothyroxine Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111228
Marketing Category Name NDA
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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