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Liothyronine sodium - 0378-3611-10 - (Liothyronine sodium)

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Drug Information of Liothyronine sodium

Product NDC: 0378-3611
Proprietary Name: Liothyronine sodium
Non Proprietary Name: Liothyronine sodium
Active Ingredient(s): 5    ug/1 & nbsp;   Liothyronine sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Liothyronine sodium

Product NDC: 0378-3611
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090326
Marketing Category: ANDA
Start Marketing Date: 20130123

Package Information of Liothyronine sodium

Package NDC: 0378-3611-10
Package Description: 1000 TABLET in 1 BOTTLE, PLASTIC (0378-3611-10)

NDC Information of Liothyronine sodium

NDC Code 0378-3611-10
Proprietary Name Liothyronine sodium
Package Description 1000 TABLET in 1 BOTTLE, PLASTIC (0378-3611-10)
Product NDC 0378-3611
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Liothyronine sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130123
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
Substance Name LIOTHYRONINE SODIUM
Strength Number 5
Strength Unit ug/1
Pharmaceutical Classes l-Triiodothyronine [EPC],Triiodothyronine [Chemical/Ingredient]

Complete Information of Liothyronine sodium


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