Home > National Drug Code (NDC) > Levothyroxine Sodium

Levothyroxine Sodium - 63629-4251-1 - (Levothyroxine Sodium)

Alphabetical Index


Drug Information of Levothyroxine Sodium

Product NDC: 63629-4251
Proprietary Name: Levothyroxine Sodium
Non Proprietary Name: Levothyroxine Sodium
Active Ingredient(s): .137    mg/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: 63629-4251
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021116
Marketing Category: NDA
Start Marketing Date: 20071001

Package Information of Levothyroxine Sodium

Package NDC: 63629-4251-1
Package Description: 30 TABLET in 1 BOTTLE (63629-4251-1)

NDC Information of Levothyroxine Sodium

NDC Code 63629-4251-1
Proprietary Name Levothyroxine Sodium
Package Description 30 TABLET in 1 BOTTLE (63629-4251-1)
Product NDC 63629-4251
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levothyroxine Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20071001
Marketing Category Name NDA
Labeler Name Bryant Ranch Prepack
Substance Name LEVOTHYROXINE SODIUM
Strength Number .137
Strength Unit mg/1
Pharmaceutical Classes l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient]

Complete Information of Levothyroxine Sodium


General Information