Tirosint - 24090-497-99 - (Levothyroxine Sodium)

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Drug Information of Tirosint

Product NDC: 24090-497
Proprietary Name: Tirosint
Non Proprietary Name: Levothyroxine Sodium
Active Ingredient(s): 125    ug/1 & nbsp;   Levothyroxine Sodium
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Tirosint

Product NDC: 24090-497
Labeler Name: Akrimax Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021924
Marketing Category: NDA
Start Marketing Date: 20100401

Package Information of Tirosint

Package NDC: 24090-497-99
Package Description: 4 BLISTER PACK in 1 CARTON (24090-497-99) > 7 CAPSULE in 1 BLISTER PACK

NDC Information of Tirosint

NDC Code 24090-497-99
Proprietary Name Tirosint
Package Description 4 BLISTER PACK in 1 CARTON (24090-497-99) > 7 CAPSULE in 1 BLISTER PACK
Product NDC 24090-497
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levothyroxine Sodium
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20100401
Marketing Category Name NDA
Labeler Name Akrimax Pharmaceuticals, LLC
Substance Name LEVOTHYROXINE SODIUM
Strength Number 125
Strength Unit ug/1
Pharmaceutical Classes l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient]

Complete Information of Tirosint


General Information