Package 16714-896-02

Brand: glipizide

Generic: glipizide
NDC Package

Package Facts

Identity

Package NDC 16714-896-02
Digits Only 1671489602
Product NDC 16714-896
Description

500 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-896-02)

Marketing

Marketing Status
Marketed Since 2018-12-01
Brand glipizide
Generic glipizide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "26f0c341-a482-4dc1-aaef-f0a92a84937c", "openfda": {"nui": ["N0000175608", "M0020795"], "upc": ["0316714896014"], "unii": ["X7WDT95N5C"], "rxcui": ["310489", "314006", "315107"], "spl_set_id": ["915636a4-092e-4e2e-9bc0-0d387d996977"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Northstar Rx LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-896-01)", "package_ndc": "16714-896-01", "marketing_start_date": "20181201"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-896-02)", "package_ndc": "16714-896-02", "marketing_start_date": "20181201"}], "brand_name": "Glipizide", "product_id": "16714-896_26f0c341-a482-4dc1-aaef-f0a92a84937c", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "16714-896", "generic_name": "Glipizide", "labeler_name": "Northstar Rx LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glipizide", "active_ingredients": [{"name": "GLIPIZIDE", "strength": "10 mg/1"}], "application_number": "ANDA203499", "marketing_category": "ANDA", "marketing_start_date": "20181201", "listing_expiration_date": "20271231"}