BRILINTA - 0186-0777-60 - (Ticagrelor)

Alphabetical Index


Drug Information of BRILINTA

Product NDC: 0186-0777
Proprietary Name: BRILINTA
Non Proprietary Name: Ticagrelor
Active Ingredient(s): 90    mg/1 & nbsp;   Ticagrelor
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of BRILINTA

Product NDC: 0186-0777
Labeler Name: AstraZeneca LP
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022433
Marketing Category: NDA
Start Marketing Date: 20110805

Package Information of BRILINTA

Package NDC: 0186-0777-60
Package Description: 60 TABLET in 1 BOTTLE (0186-0777-60)

NDC Information of BRILINTA

NDC Code 0186-0777-60
Proprietary Name BRILINTA
Package Description 60 TABLET in 1 BOTTLE (0186-0777-60)
Product NDC 0186-0777
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ticagrelor
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110805
Marketing Category Name NDA
Labeler Name AstraZeneca LP
Substance Name TICAGRELOR
Strength Number 90
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of BRILINTA


General Information