NDC 68151-2959
Anagrelide Hydrochloride
Anagrelide Hydrochloride
Anagrelide Hydrochloride is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Carilion Materials Management. The primary component is Anagrelide Hydrochloride.
| Product ID | 68151-2959_691914ba-6279-4b7c-9908-e258330fdb5b |
| NDC | 68151-2959 |
| 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 | Carilion Materials Management |
| 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 | E |
| Listing Certified Through | 2018-12-31 |