LEVOXYL - 60793-859-01 - (LEVOTHYROXINE SODIUM)

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Drug Information of LEVOXYL

Product NDC: 60793-859
Proprietary Name: LEVOXYL
Non Proprietary Name: LEVOTHYROXINE SODIUM
Active Ingredient(s): 175    ug/1 & nbsp;   LEVOTHYROXINE SODIUM
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of LEVOXYL

Product NDC: 60793-859
Labeler Name: King Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021301
Marketing Category: NDA
Start Marketing Date: 20010525

Package Information of LEVOXYL

Package NDC: 60793-859-01
Package Description: 100 TABLET in 1 BOTTLE (60793-859-01)

NDC Information of LEVOXYL

NDC Code 60793-859-01
Proprietary Name LEVOXYL
Package Description 100 TABLET in 1 BOTTLE (60793-859-01)
Product NDC 60793-859
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name LEVOTHYROXINE SODIUM
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20010525
Marketing Category Name NDA
Labeler Name King Pharmaceuticals, Inc.
Substance Name LEVOTHYROXINE SODIUM
Strength Number 175
Strength Unit ug/1
Pharmaceutical Classes l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient]

Complete Information of LEVOXYL


General Information