Synthroid - 0074-7149-90 - (Levothyroxine Sodium)

Alphabetical Index


Drug Information of Synthroid

Product NDC: 0074-7149
Proprietary Name: Synthroid
Non Proprietary Name: Levothyroxine Sodium
Active Ingredient(s): 300    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: 0074-7149
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: 0074-7149-90
Package Description: 90 TABLET in 1 BOTTLE (0074-7149-90)

NDC Information of Synthroid

NDC Code 0074-7149-90
Proprietary Name Synthroid
Package Description 90 TABLET in 1 BOTTLE (0074-7149-90)
Product NDC 0074-7149
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 300
Strength Unit ug/1
Pharmaceutical Classes l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient]

Complete Information of Synthroid


General Information