NDC 0172-5241
Anagrelide Hydrochloride
Anagrelide Hydrochloride
Anagrelide Hydrochloride is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Teva Pharmaceuticals Usa, Inc.. The primary component is Anagrelide Hydrochloride.
Product ID | 0172-5241_1840a429-9e76-4ef9-91ae-293c6e9310b6 |
NDC | 0172-5241 |
Product Type | Human Prescription Drug |
Proprietary Name | Anagrelide Hydrochloride |
Generic Name | Anagrelide Hydrochloride |
Dosage Form | Capsule |
Route of Administration | ORAL |
Marketing Start Date | 2005-04-18 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA076468 |
Labeler Name | Teva Pharmaceuticals USA, Inc. |
Substance Name | ANAGRELIDE HYDROCHLORIDE |
Active Ingredient Strength | 1 mg/1 |
Pharm Classes | Decreased Platelet Production [PE],Platelet-reducing Agent [EPC],Phosphodiesterase 3 Inhibitors [MoA] |
NDC Exclude Flag | N |
Listing Certified Through | 2022-12-31 |