Package 70954-881-10

Brand: anagrelide

Generic: anagrelide
NDC Package

Package Facts

Identity

Package NDC 70954-881-10
Digits Only 7095488110
Product NDC 70954-881
Product ID 70954-881_56b3959d-4b6b-413f-b753-9d4c20c07466
Description

100 CAPSULE in 1 BOTTLE (70954-881-10)

Marketing

Marketing Status
Marketed Since 2025-11-06
Brand anagrelide
Generic anagrelide
Sample Package No

Linked Drug Pages (1)

Anagrelide ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "56b3959d-4b6b-413f-b753-9d4c20c07466", "openfda": {"unii": ["YTM763Y5C8"], "rxcui": ["597850", "597852"], "spl_set_id": ["56b3959d-4b6b-413f-b753-9d4c20c07466"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (70954-881-10)", "package_ndc": "70954-881-10", "marketing_start_date": "20251106"}], "brand_name": "Anagrelide", "product_id": "70954-881_56b3959d-4b6b-413f-b753-9d4c20c07466", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Platelet Production [PE]", "Phosphodiesterase 3 Inhibitors [MoA]", "Platelet-reducing Agent [EPC]"], "product_ndc": "70954-881", "generic_name": "Anagrelide", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Anagrelide", "active_ingredients": [{"name": "ANAGRELIDE HYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA076811", "marketing_category": "ANDA", "marketing_start_date": "20251106", "listing_expiration_date": "20261231"}