glipizide

Generic: glipizide

Labeler: advanced rx of tennessee, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name glipizide
Generic Name glipizide
Labeler advanced rx of tennessee, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

glipizide 10 mg/1

Manufacturer
Advanced Rx of Tennessee, LLC

Identifiers & Regulatory

Product NDC 80425-0549
Product ID 80425-0549_3d87c932-9653-482e-e063-6294a90a3b84
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214874
Listing Expiration 2026-12-31
Marketing Start 2025-08-29

Pharmacologic Class

Established (EPC)
sulfonylurea [epc]
Chemical Structure
sulfonylurea compounds [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 804250549
Hyphenated Format 80425-0549

Supplemental Identifiers

RxCUI
310488
UNII
X7WDT95N5C
NUI
N0000175608 M0020795

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name glipizide (source: ndc)
Generic Name glipizide (source: ndc)
Application Number ANDA214874 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (80425-0549-1)
  • 60 TABLET in 1 BOTTLE (80425-0549-2)
  • 90 TABLET in 1 BOTTLE (80425-0549-3)
source: ndc

Packages (3)

80425-0549-1 30 TABLET in 1 BOTTLE (80425-0549-1) 80425-0549-2 60 TABLET in 1 BOTTLE (80425-0549-2) 80425-0549-3 90 TABLET in 1 BOTTLE (80425-0549-3)

Ingredients (1)

glipizide (10 mg/1)

Linked Drug Pages (1)

Glipizide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3d87c932-9653-482e-e063-6294a90a3b84", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["X7WDT95N5C"], "rxcui": ["310488"], "spl_set_id": ["3d87cc75-7a0d-46a2-e063-6294a90a6d49"], "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 (80425-0549-1)", "package_ndc": "80425-0549-1", "marketing_start_date": "20250829"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (80425-0549-2)", "package_ndc": "80425-0549-2", "marketing_start_date": "20250829"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (80425-0549-3)", "package_ndc": "80425-0549-3", "marketing_start_date": "20250829"}], "brand_name": "Glipizide", "product_id": "80425-0549_3d87c932-9653-482e-e063-6294a90a3b84", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "80425-0549", "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": "ANDA214874", "marketing_category": "ANDA", "marketing_start_date": "20250829", "listing_expiration_date": "20261231"}