Package 72162-2103-0

Brand: glipizide

Generic: glipizide
NDC Package

Package Facts

Identity

Package NDC 72162-2103-0
Digits Only 7216221030
Product NDC 72162-2103
Product ID 72162-2103_ad1b0edd-91f2-4078-904d-340bae3c9eb0
Description

1000 TABLET in 1 BOTTLE (72162-2103-0)

Marketing

Marketing Status
Marketed Since 2002-09-25
Brand glipizide
Generic glipizide
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ad1b0edd-91f2-4078-904d-340bae3c9eb0", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["X7WDT95N5C"], "rxcui": ["310490"], "spl_set_id": ["560448dd-3690-43d9-9667-925f20bb816e"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (72162-2103-0)", "package_ndc": "72162-2103-0", "marketing_start_date": "20020925"}], "brand_name": "Glipizide", "product_id": "72162-2103_ad1b0edd-91f2-4078-904d-340bae3c9eb0", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "72162-2103", "generic_name": "Glipizide", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glipizide", "active_ingredients": [{"name": "GLIPIZIDE", "strength": "5 mg/1"}], "application_number": "ANDA075795", "marketing_category": "ANDA", "marketing_start_date": "20020925", "listing_expiration_date": "20261231"}