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Anagrelide Hydrochloride
Anagrelide Hydrochloride - 0172-5241-60 - (Anagrelide Hydrochloride)
Drug Information of Anagrelide Hydrochloride
| Product NDC: | 0172-5241 |
| Proprietary Name: | Anagrelide Hydrochloride |
| 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 Anagrelide Hydrochloride
| Product NDC: | 0172-5241 |
| Labeler Name: | IVAX Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076468 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050418 |
Package Information of Anagrelide Hydrochloride
| Package NDC: | 0172-5241-60 |
| Package Description: | 100 CAPSULE in 1 BOTTLE (0172-5241-60) |
NDC Information of Anagrelide Hydrochloride
| NDC Code | 0172-5241-60 |
| Proprietary Name | Anagrelide Hydrochloride |
| Package Description | 100 CAPSULE in 1 BOTTLE (0172-5241-60) |
| Product NDC | 0172-5241 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Anagrelide Hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20050418 |
| Marketing Category Name | ANDA |
| Labeler Name | IVAX Pharmaceuticals, 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] |
