Synthroid - 43063-178-90 - (Levothyroxine Sodium)

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Drug Information of Synthroid

Product NDC: 43063-178
Proprietary Name: Synthroid
Non Proprietary Name: Levothyroxine Sodium
Active Ingredient(s): 125    ug/1 & nbsp;   Levothyroxine Sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Synthroid

Product NDC: 43063-178
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021402
Marketing Category: NDA
Start Marketing Date: 20020724

Package Information of Synthroid

Package NDC: 43063-178-90
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (43063-178-90)

NDC Information of Synthroid

NDC Code 43063-178-90
Proprietary Name Synthroid
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (43063-178-90)
Product NDC 43063-178
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levothyroxine Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20020724
Marketing Category Name NDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name LEVOTHYROXINE SODIUM
Strength Number 125
Strength Unit ug/1
Pharmaceutical Classes l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient]

Complete Information of Synthroid


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