Package 42291-321-01

Brand: hydroxyurea

Generic: hydroxyurea
NDC Package

Package Facts

Identity

Package NDC 42291-321-01
Digits Only 4229132101
Product NDC 42291-321
Product ID 42291-321_4133de1c-b333-3b84-e063-6294a90a2432
Description

100 CAPSULE in 1 BOTTLE (42291-321-01)

Marketing

Marketing Status
Marketed Since 2013-07-23
Brand hydroxyurea
Generic hydroxyurea
Sample Package No

Linked Drug Pages (1)

HYDROXYUREA ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4133de1c-b333-3b84-e063-6294a90a2432", "openfda": {"nui": ["N0000180853", "M0022315"], "unii": ["X6Q56QN5QC"], "rxcui": ["197797"], "spl_set_id": ["862583ff-6d5c-3f7d-e3bd-352fb0400928"], "pharm_class_cs": ["Urea [CS]"], "pharm_class_epc": ["Antimetabolite [EPC]"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (42291-321-01)", "package_ndc": "42291-321-01", "marketing_start_date": "20130723"}], "brand_name": "HYDROXYUREA", "product_id": "42291-321_4133de1c-b333-3b84-e063-6294a90a2432", "dosage_form": "CAPSULE", "pharm_class": ["Antimetabolite [EPC]", "Urea [CS]"], "product_ndc": "42291-321", "generic_name": "Hydroxyurea", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROXYUREA", "active_ingredients": [{"name": "HYDROXYUREA", "strength": "500 mg/1"}], "application_number": "ANDA075143", "marketing_category": "ANDA", "marketing_start_date": "20130723", "listing_expiration_date": "20261231"}