Anagrelide Hydrochloride - Anagrelide Hydrochloride
Navigation: NDC > Supplier starting with: I > IVAX PHARMACEUTICALS, INC.| Field | Value |
|---|---|
| NDC Code: | 0172-5240 |
| Proprietary Name: | Anagrelide Hydrochloride |
| Suffix: | |
| Non-Proprietary Name: | Anagrelide Hydrochloride |
| Dosage Form: | CAPSULE |
| Method: | ORAL |
| Original Marketing Date: | 18-04-2005 |
| Category Name: | ANDA |
| Application Number: | ANDA076468 |
| Labeler: | IVAX PHARMACEUTICALS, INC. |
| Substance Name: | ANAGRELIDE HYDROCHLORIDE |
| Active Numerator Strength: | 1 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Decreased Platelet Production [PE],Platelet-reducing Agent [EPC],Phosphodiesterase 3 Inhibitors [MoA] |
| DEA Schedule: |