Letairis - 61958-0801-2 - (AMBRISENTAN)

Alphabetical Index


Drug Information of Letairis

Product NDC: 61958-0801
Proprietary Name: Letairis
Non Proprietary Name: AMBRISENTAN
Active Ingredient(s): 5    mg/1 & nbsp;   AMBRISENTAN
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Letairis

Product NDC: 61958-0801
Labeler Name: Gilead Sciences, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022081
Marketing Category: NDA
Start Marketing Date: 20070615

Package Information of Letairis

Package NDC: 61958-0801-2
Package Description: 3 BLISTER PACK in 1 CARTON (61958-0801-2) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Letairis

NDC Code 61958-0801-2
Proprietary Name Letairis
Package Description 3 BLISTER PACK in 1 CARTON (61958-0801-2) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 61958-0801
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name AMBRISENTAN
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070615
Marketing Category Name NDA
Labeler Name Gilead Sciences, Inc
Substance Name AMBRISENTAN
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Endothelin Receptor Antagonist [EPC],Endothelin Receptor Antagonists [MoA]

Complete Information of Letairis


General Information