Package 72162-2102-0

Brand: glipizide

Generic: glipizide
NDC Package

Package Facts

Identity

Package NDC 72162-2102-0
Digits Only 7216221020
Product NDC 72162-2102
Product ID 72162-2102_728036ca-06bb-4034-b9a3-77b4b26f0e6f
Description

1000 TABLET in 1 BOTTLE (72162-2102-0)

Marketing

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

Linked Drug Pages (1)

Glipizide ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "728036ca-06bb-4034-b9a3-77b4b26f0e6f", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["X7WDT95N5C"], "rxcui": ["310488"], "spl_set_id": ["be20727f-2724-457a-89ac-aa96604a0015"], "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 (72162-2102-0)", "package_ndc": "72162-2102-0", "marketing_start_date": "20020925"}], "brand_name": "Glipizide", "product_id": "72162-2102_728036ca-06bb-4034-b9a3-77b4b26f0e6f", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "72162-2102", "generic_name": "Glipizide", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glipizide", "active_ingredients": [{"name": "GLIPIZIDE", "strength": "10 mg/1"}], "application_number": "ANDA075795", "marketing_category": "ANDA", "marketing_start_date": "20020925", "listing_expiration_date": "20261231"}