Levothroid - 55289-777-30 - (levothyroxine sodium)

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Drug Information of Levothroid

Product NDC: 55289-777
Proprietary Name: Levothroid
Non Proprietary Name: levothyroxine sodium
Active Ingredient(s): 125    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: 55289-777
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021116
Marketing Category: NDA
Start Marketing Date: 20101018

Package Information of Levothroid

Package NDC: 55289-777-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (55289-777-30)

NDC Information of Levothroid

NDC Code 55289-777-30
Proprietary Name Levothroid
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (55289-777-30)
Product NDC 55289-777
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name levothyroxine sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101018
Marketing Category Name NDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name LEVOTHYROXINE SODIUM
Strength Number 125
Strength Unit ug/1
Pharmaceutical Classes l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient]

Complete Information of Levothroid


General Information