Synthroid - 0074-7069-71 - (Levothyroxine Sodium)

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Drug Information of Synthroid

Product NDC: 0074-7069
Proprietary Name: Synthroid
Non Proprietary Name: Levothyroxine Sodium
Active Ingredient(s): 150    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: 0074-7069
Labeler Name: Abbott Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021402
Marketing Category: NDA
Start Marketing Date: 20020724

Package Information of Synthroid

Package NDC: 0074-7069-71
Package Description: 4 BLISTER PACK in 1 CARTON (0074-7069-71) > 7 TABLET in 1 BLISTER PACK

NDC Information of Synthroid

NDC Code 0074-7069-71
Proprietary Name Synthroid
Package Description 4 BLISTER PACK in 1 CARTON (0074-7069-71) > 7 TABLET in 1 BLISTER PACK
Product NDC 0074-7069
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 Abbott Laboratories
Substance Name LEVOTHYROXINE SODIUM
Strength Number 150
Strength Unit ug/1
Pharmaceutical Classes l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient]

Complete Information of Synthroid


General Information