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Levothyroxine Sodium - 63629-1839-4 - (Levothyroxine Sodium)

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Drug Information of Levothyroxine Sodium

Product NDC: 63629-1839
Proprietary Name: Levothyroxine Sodium
Non Proprietary Name: Levothyroxine Sodium
Active Ingredient(s): .1    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: 63629-1839
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021210
Marketing Category: NDA
Start Marketing Date: 20031201

Package Information of Levothyroxine Sodium

Package NDC: 63629-1839-4
Package Description: 7 TABLET in 1 BOTTLE (63629-1839-4)

NDC Information of Levothyroxine Sodium

NDC Code 63629-1839-4
Proprietary Name Levothyroxine Sodium
Package Description 7 TABLET in 1 BOTTLE (63629-1839-4)
Product NDC 63629-1839
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 Bryant Ranch Prepack
Substance Name LEVOTHYROXINE SODIUM
Strength Number .1
Strength Unit mg/1
Pharmaceutical Classes l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient]

Complete Information of Levothyroxine Sodium


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