Package 55111-626-60
Brand: zafirlukast
Generic: zafirlukastPackage Facts
Identity
Package NDC
55111-626-60
Digits Only
5511162660
Product NDC
55111-626
Description
60 TABLET, FILM COATED in 1 BOTTLE (55111-626-60)
Marketing
Marketing Status
Brand
zafirlukast
Generic
zafirlukast
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b5fb9efb-3369-e1f9-384c-bd22e8ecad92", "openfda": {"nui": ["N0000175777", "N0000000083", "N0000185504"], "upc": ["0355111625605", "0355111626602"], "unii": ["XZ629S5L50"], "rxcui": ["199655", "313758"], "spl_set_id": ["6ccb96af-2647-9206-5eee-49a825d32488"], "pharm_class_epc": ["Leukotriene Receptor Antagonist [EPC]"], "pharm_class_moa": ["Leukotriene Receptor Antagonists [MoA]", "Cytochrome P450 2C9 Inhibitors [MoA]"], "manufacturer_name": ["Dr. Reddys Laboratories Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (55111-626-01)", "package_ndc": "55111-626-01", "marketing_start_date": "20101118"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (55111-626-05)", "package_ndc": "55111-626-05", "marketing_start_date": "20101118"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (55111-626-30)", "package_ndc": "55111-626-30", "marketing_start_date": "20101118"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (55111-626-60)", "package_ndc": "55111-626-60", "marketing_start_date": "20101118"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (55111-626-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-626-79)", "package_ndc": "55111-626-78", "marketing_start_date": "20101118"}], "brand_name": "Zafirlukast", "product_id": "55111-626_b5fb9efb-3369-e1f9-384c-bd22e8ecad92", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2C9 Inhibitors [MoA]", "Leukotriene Receptor Antagonist [EPC]", "Leukotriene Receptor Antagonists [MoA]"], "product_ndc": "55111-626", "generic_name": "Zafirlukast", "labeler_name": "Dr. Reddys Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zafirlukast", "active_ingredients": [{"name": "ZAFIRLUKAST", "strength": "20 mg/1"}], "application_number": "ANDA090372", "marketing_category": "ANDA", "marketing_start_date": "20101118", "listing_expiration_date": "20261231"}