Levothroid - 0456-1320-01 - (LEVOTHYROXINE SODIUM)

Alphabetical Index


Drug Information of Levothroid

Product NDC: 0456-1320
Proprietary Name: Levothroid
Non Proprietary Name: LEVOTHYROXINE SODIUM
Active Ingredient(s): 25    ug/1 & nbsp;   LEVOTHYROXINE SODIUM
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Levothroid

Product NDC: 0456-1320
Labeler Name: Forest Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021116
Marketing Category: NDA
Start Marketing Date: 20031016

Package Information of Levothroid

Package NDC: 0456-1320-01
Package Description: 100 TABLET in 1 BOTTLE (0456-1320-01)

NDC Information of Levothroid

NDC Code 0456-1320-01
Proprietary Name Levothroid
Package Description 100 TABLET in 1 BOTTLE (0456-1320-01)
Product NDC 0456-1320
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name LEVOTHYROXINE SODIUM
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20031016
Marketing Category Name NDA
Labeler Name Forest Laboratories, Inc.
Substance Name LEVOTHYROXINE SODIUM
Strength Number 25
Strength Unit ug/1
Pharmaceutical Classes l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient]

Complete Information of Levothroid


General Information