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LEVOTHYROXINE SODIUM - 51138-046-30 - (Levothyroxine Sodium)

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Drug Information of LEVOTHYROXINE SODIUM

Product NDC: 51138-046
Proprietary Name: LEVOTHYROXINE SODIUM
Non Proprietary Name: Levothyroxine Sodium
Active Ingredient(s): .137    mg/1 & nbsp;   Levothyroxine Sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of LEVOTHYROXINE SODIUM

Product NDC: 51138-046
Labeler Name: Med-Health Pharma, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021210
Marketing Category: NDA
Start Marketing Date: 20110101

Package Information of LEVOTHYROXINE SODIUM

Package NDC: 51138-046-30
Package Description: 30 TABLET in 1 BOTTLE (51138-046-30)

NDC Information of LEVOTHYROXINE SODIUM

NDC Code 51138-046-30
Proprietary Name LEVOTHYROXINE SODIUM
Package Description 30 TABLET in 1 BOTTLE (51138-046-30)
Product NDC 51138-046
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levothyroxine Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110101
Marketing Category Name NDA
Labeler Name Med-Health Pharma, LLC
Substance Name LEVOTHYROXINE SODIUM
Strength Number .137
Strength Unit mg/1
Pharmaceutical Classes l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient]

Complete Information of LEVOTHYROXINE SODIUM


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