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Levothyroxine Sodium - 51079-441-20 - (levothyroxine sodium)

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Drug Information of Levothyroxine Sodium

Product NDC: 51079-441
Proprietary Name: Levothyroxine Sodium
Non Proprietary Name: levothyroxine sodium
Active Ingredient(s): 75    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: 51079-441
Labeler Name: UDL Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076187
Marketing Category: ANDA
Start Marketing Date: 20101029

Package Information of Levothyroxine Sodium

Package NDC: 51079-441-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-441-20) > 1 TABLET in 1 BLISTER PACK (51079-441-01)

NDC Information of Levothyroxine Sodium

NDC Code 51079-441-20
Proprietary Name Levothyroxine Sodium
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-441-20) > 1 TABLET in 1 BLISTER PACK (51079-441-01)
Product NDC 51079-441
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name levothyroxine sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101029
Marketing Category Name ANDA
Labeler Name UDL Laboratories, Inc.
Substance Name LEVOTHYROXINE SODIUM
Strength Number 75
Strength Unit ug/1
Pharmaceutical Classes l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient]

Complete Information of Levothyroxine Sodium


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