Cytomel - 54868-1750-2 - (liothyronine sodium)

Alphabetical Index


Drug Information of Cytomel

Product NDC: 54868-1750
Proprietary Name: Cytomel
Non Proprietary Name: liothyronine sodium
Active Ingredient(s): 25    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: 54868-1750
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA010379
Marketing Category: NDA
Start Marketing Date: 20021230

Package Information of Cytomel

Package NDC: 54868-1750-2
Package Description: 10 TABLET in 1 BOTTLE, PLASTIC (54868-1750-2)

NDC Information of Cytomel

NDC Code 54868-1750-2
Proprietary Name Cytomel
Package Description 10 TABLET in 1 BOTTLE, PLASTIC (54868-1750-2)
Product NDC 54868-1750
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name liothyronine sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20021230
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name LIOTHYRONINE SODIUM
Strength Number 25
Strength Unit ug/1
Pharmaceutical Classes l-Triiodothyronine [EPC],Triiodothyronine [Chemical/Ingredient]

Complete Information of Cytomel


General Information