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Liothyronine Sodium - 43063-252-30 - (Liothyronine Sodium)

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Drug Information of Liothyronine Sodium

Product NDC: 43063-252
Proprietary Name: Liothyronine Sodium
Non Proprietary Name: Liothyronine Sodium
Active Ingredient(s): 50    ug/1 & nbsp;   Liothyronine Sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Liothyronine Sodium

Product NDC: 43063-252
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090097
Marketing Category: ANDA
Start Marketing Date: 20090323

Package Information of Liothyronine Sodium

Package NDC: 43063-252-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (43063-252-30)

NDC Information of Liothyronine Sodium

NDC Code 43063-252-30
Proprietary Name Liothyronine Sodium
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (43063-252-30)
Product NDC 43063-252
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Liothyronine Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090323
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name LIOTHYRONINE SODIUM
Strength Number 50
Strength Unit ug/1
Pharmaceutical Classes l-Triiodothyronine [EPC],Triiodothyronine [Chemical/Ingredient]

Complete Information of Liothyronine Sodium


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