Package 72789-510-30

Brand: glipizide

Generic: glipizide
NDC Package

Package Facts

Identity

Package NDC 72789-510-30
Digits Only 7278951030
Product NDC 72789-510
Description

30 TABLET in 1 BOTTLE, PLASTIC (72789-510-30)

Marketing

Marketing Status
Marketed Since 2025-05-23
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": "35d2a5a0-9016-e44c-e063-6394a90aec87", "openfda": {"nui": ["N0000175608", "M0020795"], "upc": ["0372789510309"], "unii": ["X7WDT95N5C"], "rxcui": ["310488"], "spl_set_id": ["c8cfd137-7b41-460f-a463-141c9d1985ff"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-510-30)", "package_ndc": "72789-510-30", "marketing_start_date": "20250523"}], "brand_name": "Glipizide", "product_id": "72789-510_35d2a5a0-9016-e44c-e063-6394a90aec87", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "72789-510", "generic_name": "Glipizide", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glipizide", "active_ingredients": [{"name": "GLIPIZIDE", "strength": "10 mg/1"}], "application_number": "ANDA214874", "marketing_category": "ANDA", "marketing_start_date": "20231003", "listing_expiration_date": "20261231"}