Package 0904-6939-61

Brand: hydroxyurea

Generic: hydroxyurea
NDC Package

Package Facts

Identity

Package NDC 0904-6939-61
Digits Only 0904693961
Product NDC 0904-6939
Description

100 BLISTER PACK in 1 CARTON (0904-6939-61) / 1 CAPSULE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 1999-02-24
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": "554e6427-7d26-4f99-b69b-10468b9bb014", "openfda": {"nui": ["N0000180853", "M0022315"], "unii": ["X6Q56QN5QC"], "rxcui": ["197797"], "spl_set_id": ["e76fd60e-7644-48c5-9857-3608a045000b"], "pharm_class_cs": ["Urea [CS]"], "pharm_class_epc": ["Antimetabolite [EPC]"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6939-61)  / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "0904-6939-61", "marketing_start_date": "19990224"}], "brand_name": "Hydroxyurea", "product_id": "0904-6939_554e6427-7d26-4f99-b69b-10468b9bb014", "dosage_form": "CAPSULE", "pharm_class": ["Antimetabolite [EPC]", "Urea [CS]"], "product_ndc": "0904-6939", "generic_name": "Hydroxyurea", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyurea", "active_ingredients": [{"name": "HYDROXYUREA", "strength": "500 mg/1"}], "application_number": "ANDA075340", "marketing_category": "ANDA", "marketing_start_date": "19990224", "listing_expiration_date": "20261231"}