Anagrelide 70954-0879
Product NDC
70954-0879- Manufacturer
- Ani Pharmaceuticals, Inc.
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- November 6, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA076811
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Anagrelide Hydrochloride | .5 mg/1 |
Drug Class
Decreased Platelet Production [PE]Phosphodiesterase 3 Inhibitors [MoA]Platelet-reducing Agent [EPC]
Packaging Options(1)
100 CAPSULE in 1 BOTTLE (70954-879-10)