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Levothyroxine Sodium - 55289-085-30 - (levothyroxine sodium)

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Drug Information of Levothyroxine Sodium

Product NDC: 55289-085
Proprietary Name: Levothyroxine Sodium
Non Proprietary Name: levothyroxine sodium
Active Ingredient(s): 50    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: 55289-085
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076187
Marketing Category: ANDA
Start Marketing Date: 20100118

Package Information of Levothyroxine Sodium

Package NDC: 55289-085-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (55289-085-30)

NDC Information of Levothyroxine Sodium

NDC Code 55289-085-30
Proprietary Name Levothyroxine Sodium
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (55289-085-30)
Product NDC 55289-085
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name levothyroxine sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100118
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name LEVOTHYROXINE SODIUM
Strength Number 50
Strength Unit ug/1
Pharmaceutical Classes l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient]

Complete Information of Levothyroxine Sodium


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