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Levothyroxine Sodium - 0527-1341-10 - (Levothyroxine Sodium)

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Drug Information of Levothyroxine Sodium

Product NDC: 0527-1341
Proprietary Name: Levothyroxine Sodium
Non Proprietary Name: Levothyroxine Sodium
Active Ingredient(s): .025    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: 0527-1341
Labeler Name: Lannett Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021210
Marketing Category: NDA
Start Marketing Date: 20031201

Package Information of Levothyroxine Sodium

Package NDC: 0527-1341-10
Package Description: 1000 TABLET in 1 BOTTLE, PLASTIC (0527-1341-10)

NDC Information of Levothyroxine Sodium

NDC Code 0527-1341-10
Proprietary Name Levothyroxine Sodium
Package Description 1000 TABLET in 1 BOTTLE, PLASTIC (0527-1341-10)
Product NDC 0527-1341
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levothyroxine Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20031201
Marketing Category Name NDA
Labeler Name Lannett Company, Inc.
Substance Name LEVOTHYROXINE SODIUM
Strength Number .025
Strength Unit mg/1
Pharmaceutical Classes l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient]

Complete Information of Levothyroxine Sodium


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