Strength
1 mg/1
Manufacturer
ANI Pharmaceuticals, Inc.NDC
70954088110
Classification
Generic
Dosage Form
CAPSULE
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
ANAGRELIDE HYDROCHLORIDEApproval Type
Generic (ANDA)
FDA Application
ANDA076811On Market Since
11/6/2025
Pharmacological Classes
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