glipizide

Generic: glipizide

Labeler: oxford pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name glipizide
Generic Name glipizide
Labeler oxford pharmaceuticals, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

glipizide 10 mg/1

Manufacturer
Oxford Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 69584-310
Product ID 69584-310_496b39ed-3ca0-4265-a401-674fe6d4a0d1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074378
Listing Expiration 2026-12-31
Marketing Start 2025-05-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69584310
Hyphenated Format 69584-310

Supplemental Identifiers

RxCUI
310488 310490
UNII
X7WDT95N5C
NUI
N0000175608 M0020795

Packaging Origin

Original Packager
true

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 ANDA074378 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (69584-310-10)
  • 500 TABLET in 1 BOTTLE (69584-310-50)
  • 1000 TABLET in 1 BOTTLE (69584-310-90)
source: ndc

Packages (3)

69584-310-10 100 TABLET in 1 BOTTLE (69584-310-10) 69584-310-50 500 TABLET in 1 BOTTLE (69584-310-50) 69584-310-90 1000 TABLET in 1 BOTTLE (69584-310-90)

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": "496b39ed-3ca0-4265-a401-674fe6d4a0d1", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["X7WDT95N5C"], "rxcui": ["310488", "310490"], "spl_set_id": ["87cd4930-ba68-4acf-bf74-619c477b557d"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Oxford Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69584-310-10)", "package_ndc": "69584-310-10", "marketing_start_date": "20250501"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (69584-310-50)", "package_ndc": "69584-310-50", "marketing_start_date": "20250501"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (69584-310-90)", "package_ndc": "69584-310-90", "marketing_start_date": "20250501"}], "brand_name": "Glipizide", "product_id": "69584-310_496b39ed-3ca0-4265-a401-674fe6d4a0d1", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "69584-310", "generic_name": "Glipizide", "labeler_name": "Oxford Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glipizide", "active_ingredients": [{"name": "GLIPIZIDE", "strength": "10 mg/1"}], "application_number": "ANDA074378", "marketing_category": "ANDA", "marketing_start_date": "20250501", "listing_expiration_date": "20261231"}