Package 67184-0607-1

Brand: hydroxyurea

Generic: hydroxyurea
NDC Package

Package Facts

Identity

Package NDC 67184-0607-1
Digits Only 6718406071
Product NDC 67184-0607
Description

100 CAPSULE in 1 BOTTLE (67184-0607-1)

Marketing

Marketing Status
Marketed Since 2024-03-06
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": "a252a0db-b5ce-49d2-b29d-461b34a41479", "openfda": {"nui": ["N0000180853", "M0022315"], "upc": ["0367184060719"], "unii": ["X6Q56QN5QC"], "rxcui": ["197797"], "spl_set_id": ["4cd244d4-bd4a-41c8-b072-c2135787d412"], "pharm_class_cs": ["Urea [CS]"], "pharm_class_epc": ["Antimetabolite [EPC]"], "manufacturer_name": ["Qilu Pharmaceutical Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (67184-0607-1)", "package_ndc": "67184-0607-1", "marketing_start_date": "20240306"}], "brand_name": "HYDROXYUREA", "product_id": "67184-0607_a252a0db-b5ce-49d2-b29d-461b34a41479", "dosage_form": "CAPSULE", "pharm_class": ["Antimetabolite [EPC]", "Urea [CS]"], "product_ndc": "67184-0607", "generic_name": "HYDROXYUREA", "labeler_name": "Qilu Pharmaceutical Co., Ltd.", "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": "20240306", "listing_expiration_date": "20261231"}