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