Agrylin - 54092-063-01 - (anagrelide hydrochloride)

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Drug Information of Agrylin

Product NDC: 54092-063
Proprietary Name: Agrylin
Non Proprietary Name: anagrelide hydrochloride
Active Ingredient(s): .5    mg/1 & nbsp;   anagrelide hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Agrylin

Product NDC: 54092-063
Labeler Name: Shire US Manufacturing Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020333
Marketing Category: NDA
Start Marketing Date: 19970314

Package Information of Agrylin

Package NDC: 54092-063-01
Package Description: 100 CAPSULE in 1 BOTTLE (54092-063-01)

NDC Information of Agrylin

NDC Code 54092-063-01
Proprietary Name Agrylin
Package Description 100 CAPSULE in 1 BOTTLE (54092-063-01)
Product NDC 54092-063
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name anagrelide hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19970314
Marketing Category Name NDA
Labeler Name Shire US Manufacturing Inc.
Substance Name ANAGRELIDE HYDROCHLORIDE
Strength Number .5
Strength Unit mg/1
Pharmaceutical Classes Decreased Platelet Production [PE],Platelet-reducing Agent [EPC],Phosphodiesterase 3 Inhibitors [MoA]

Complete Information of Agrylin


General Information