Package 0781-5667-10

Brand: voriconazole

Generic: voriconazole
NDC Package

Package Facts

Identity

Package NDC 0781-5667-10
Digits Only 0781566710
Product NDC 0781-5667
Description

1000 TABLET, FILM COATED in 1 BOTTLE (0781-5667-10)

Marketing

Marketing Status
Marketed Since 2011-12-12
Brand voriconazole
Generic voriconazole
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4be02cb0-ecd6-4f37-b33c-69696402c20d", "openfda": {"nui": ["N0000175487", "M0002083", "N0000182141", "N0000182140", "N0000185504"], "upc": ["0307815668310", "0307815667313"], "unii": ["JFU09I87TR"], "rxcui": ["349434", "349435"], "spl_set_id": ["e2b3c0b3-02a6-45c3-a8ea-05d210dc9108"], "pharm_class_cs": ["Azoles [CS]"], "pharm_class_epc": ["Azole Antifungal [EPC]"], "pharm_class_moa": ["Cytochrome P450 3A4 Inhibitors [MoA]", "Cytochrome P450 2C19 Inhibitors [MoA]", "Cytochrome P450 2C9 Inhibitors [MoA]"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (0781-5667-05)", "package_ndc": "0781-5667-05", "marketing_start_date": "20111212"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (0781-5667-10)", "package_ndc": "0781-5667-10", "marketing_start_date": "20111212"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (0781-5667-13)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (0781-5667-06)", "package_ndc": "0781-5667-13", "marketing_start_date": "20111212"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (0781-5667-31)", "package_ndc": "0781-5667-31", "marketing_start_date": "20111212"}], "brand_name": "voriconazole", "product_id": "0781-5667_4be02cb0-ecd6-4f37-b33c-69696402c20d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Azole Antifungal [EPC]", "Azoles [CS]", "Cytochrome P450 2C19 Inhibitors [MoA]", "Cytochrome P450 2C9 Inhibitors [MoA]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "0781-5667", "generic_name": "voriconazole", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "voriconazole", "active_ingredients": [{"name": "VORICONAZOLE", "strength": "50 mg/1"}], "application_number": "ANDA200265", "marketing_category": "ANDA", "marketing_start_date": "20111212", "listing_expiration_date": "20261231"}