Cytomel - 60793-117-01 - (LIOTHYRONINE SODIUM)

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Drug Information of Cytomel

Product NDC: 60793-117
Proprietary Name: Cytomel
Non Proprietary Name: LIOTHYRONINE SODIUM
Active Ingredient(s): 50    ug/1 & nbsp;   LIOTHYRONINE SODIUM
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Cytomel

Product NDC: 60793-117
Labeler Name: King Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA010379
Marketing Category: NDA
Start Marketing Date: 19560508

Package Information of Cytomel

Package NDC: 60793-117-01
Package Description: 100 TABLET in 1 BOTTLE (60793-117-01)

NDC Information of Cytomel

NDC Code 60793-117-01
Proprietary Name Cytomel
Package Description 100 TABLET in 1 BOTTLE (60793-117-01)
Product NDC 60793-117
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name LIOTHYRONINE SODIUM
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19560508
Marketing Category Name NDA
Labeler Name King Pharmaceuticals, Inc.
Substance Name LIOTHYRONINE SODIUM
Strength Number 50
Strength Unit ug/1
Pharmaceutical Classes l-Triiodothyronine [EPC],Triiodothyronine [Chemical/Ingredient]

Complete Information of Cytomel


General Information