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LIOTHYRONINE SODIUM - 0179-0019-70 - (LIOTHYRONINE SODIUM)

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Drug Information of LIOTHYRONINE SODIUM

Product NDC: 0179-0019
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: 0179-0019
Labeler Name: KAISER FOUNDATION HOSPITALS
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090097
Marketing Category: ANDA
Start Marketing Date: 20090828

Package Information of LIOTHYRONINE SODIUM

Package NDC: 0179-0019-70
Package Description: 30 TABLET in 1 BOX, UNIT-DOSE (0179-0019-70)

NDC Information of LIOTHYRONINE SODIUM

NDC Code 0179-0019-70
Proprietary Name LIOTHYRONINE SODIUM
Package Description 30 TABLET in 1 BOX, UNIT-DOSE (0179-0019-70)
Product NDC 0179-0019
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name LIOTHYRONINE SODIUM
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090828
Marketing Category Name ANDA
Labeler Name KAISER FOUNDATION HOSPITALS
Substance Name LIOTHYRONINE SODIUM
Strength Number 5
Strength Unit ug/1
Pharmaceutical Classes l-Triiodothyronine [EPC],Triiodothyronine [Chemical/Ingredient]

Complete Information of LIOTHYRONINE SODIUM


General Information