UNITHROID - 0527-1370-01 - (levothyroxine sodium)

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Drug Information of UNITHROID

Product NDC: 0527-1370
Proprietary Name: UNITHROID
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 UNITHROID

Product NDC: 0527-1370
Labeler Name: Lannett Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021210
Marketing Category: NDA
Start Marketing Date: 20000821

Package Information of UNITHROID

Package NDC: 0527-1370-01
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (0527-1370-01)

NDC Information of UNITHROID

NDC Code 0527-1370-01
Proprietary Name UNITHROID
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (0527-1370-01)
Product NDC 0527-1370
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name levothyroxine sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20000821
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 UNITHROID


General Information