Package 68382-186-10
Brand: glipizide and metformin hydrochloride
Generic: glipizide and metformin hydrochloridePackage Facts
Identity
Package NDC
68382-186-10
Digits Only
6838218610
Product NDC
68382-186
Description
1000 TABLET, FILM COATED in 1 BOTTLE (68382-186-10)
Marketing
Marketing Status
Brand
glipizide and metformin hydrochloride
Generic
glipizide and metformin hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "cf07fef0-8b0c-4673-8a46-afbf1d21d0b7", "openfda": {"nui": ["N0000175608", "M0020795"], "upc": ["0368382184016"], "unii": ["X7WDT95N5C", "786Z46389E"], "rxcui": ["861731", "861736", "861740"], "spl_set_id": ["1b18b903-eb52-4d08-b4a5-f984957eb116"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68382-186-01)", "package_ndc": "68382-186-01", "marketing_start_date": "20160505"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (68382-186-10)", "package_ndc": "68382-186-10", "marketing_start_date": "20160505"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68382-186-16)", "package_ndc": "68382-186-16", "marketing_start_date": "20160505"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (68382-186-77) / 10 TABLET, FILM COATED in 1 BLISTER PACK (68382-186-30)", "package_ndc": "68382-186-77", "marketing_start_date": "20160505"}], "brand_name": "Glipizide and Metformin Hydrochloride", "product_id": "68382-186_cf07fef0-8b0c-4673-8a46-afbf1d21d0b7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]", "Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "68382-186", "generic_name": "Glipizide and Metformin Hydrochloride", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glipizide and Metformin Hydrochloride", "active_ingredients": [{"name": "GLIPIZIDE", "strength": "5 mg/1"}, {"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA078905", "marketing_category": "ANDA", "marketing_start_date": "20160505", "listing_expiration_date": "20261231"}