Package 80425-0437-3

Brand: glipizide

Generic: glipizide
NDC Package

Package Facts

Identity

Package NDC 80425-0437-3
Digits Only 8042504373
Product NDC 80425-0437
Description

90 TABLET in 1 BOTTLE (80425-0437-3)

Marketing

Marketing Status
Marketed Since 2024-09-03
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": "213c486b-f952-bffc-e063-6394a90a164e", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["X7WDT95N5C"], "rxcui": ["310488"], "spl_set_id": ["213c4e61-9bb7-9d1b-e063-6394a90a7339"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (80425-0437-1)", "package_ndc": "80425-0437-1", "marketing_start_date": "20240903"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (80425-0437-2)", "package_ndc": "80425-0437-2", "marketing_start_date": "20240903"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (80425-0437-3)", "package_ndc": "80425-0437-3", "marketing_start_date": "20240903"}], "brand_name": "Glipizide", "product_id": "80425-0437_213c486b-f952-bffc-e063-6394a90a164e", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "80425-0437", "generic_name": "Glipizide", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glipizide", "active_ingredients": [{"name": "GLIPIZIDE", "strength": "10 mg/1"}], "application_number": "ANDA074497", "marketing_category": "ANDA", "marketing_start_date": "20240903", "listing_expiration_date": "20261231"}