LEVOXYL - 60793-857-10 - (LEVOTHYROXINE SODIUM)

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Drug Information of LEVOXYL

Product NDC: 60793-857
Proprietary Name: LEVOXYL
Non Proprietary Name: LEVOTHYROXINE SODIUM
Active Ingredient(s): 137    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: 60793-857
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: 60793-857-10
Package Description: 1000 TABLET in 1 BOTTLE (60793-857-10)

NDC Information of LEVOXYL

NDC Code 60793-857-10
Proprietary Name LEVOXYL
Package Description 1000 TABLET in 1 BOTTLE (60793-857-10)
Product NDC 60793-857
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 137
Strength Unit ug/1
Pharmaceutical Classes l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient]

Complete Information of LEVOXYL


General Information