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Levothyroxine Sodium - 53808-0608-1 - (levothyroxine sodium)

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Drug Information of Levothyroxine Sodium

Product NDC: 53808-0608
Proprietary Name: Levothyroxine Sodium
Non Proprietary Name: levothyroxine sodium
Active Ingredient(s): 100    ug/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: 53808-0608
Labeler Name: State of Florida DOH Central Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076187
Marketing Category: ANDA
Start Marketing Date: 20090701

Package Information of Levothyroxine Sodium

Package NDC: 53808-0608-1
Package Description: 30 TABLET in 1 BLISTER PACK (53808-0608-1)

NDC Information of Levothyroxine Sodium

NDC Code 53808-0608-1
Proprietary Name Levothyroxine Sodium
Package Description 30 TABLET in 1 BLISTER PACK (53808-0608-1)
Product NDC 53808-0608
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name levothyroxine sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090701
Marketing Category Name ANDA
Labeler Name State of Florida DOH Central Pharmacy
Substance Name LEVOTHYROXINE SODIUM
Strength Number 100
Strength Unit ug/1
Pharmaceutical Classes l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient]

Complete Information of Levothyroxine Sodium


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