Package 70069-820-01

Brand: hydroxyurea

Generic: hydroxyurea
NDC Package

Package Facts

Identity

Package NDC 70069-820-01
Digits Only 7006982001
Product NDC 70069-820
Description

100 CAPSULE in 1 BOTTLE (70069-820-01)

Marketing

Marketing Status
Marketed Since 2024-06-18
Brand hydroxyurea
Generic hydroxyurea
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1c41acb0-9bab-4c8f-b383-2707e88a120c", "openfda": {"nui": ["N0000180853", "M0022315"], "upc": ["0370069820018"], "unii": ["X6Q56QN5QC"], "rxcui": ["197797"], "spl_set_id": ["9752a347-b42c-44d5-8fd1-c538f7f239dc"], "pharm_class_cs": ["Urea [CS]"], "pharm_class_epc": ["Antimetabolite [EPC]"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (70069-820-01)", "package_ndc": "70069-820-01", "marketing_start_date": "20240618"}], "brand_name": "HYDROXYUREA", "product_id": "70069-820_1c41acb0-9bab-4c8f-b383-2707e88a120c", "dosage_form": "CAPSULE", "pharm_class": ["Antimetabolite [EPC]", "Urea [CS]"], "product_ndc": "70069-820", "generic_name": "HYDROXYUREA", "labeler_name": "Somerset Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROXYUREA", "active_ingredients": [{"name": "HYDROXYUREA", "strength": "500 mg/1"}], "application_number": "ANDA218021", "marketing_category": "ANDA", "marketing_start_date": "20240618", "listing_expiration_date": "20261231"}