glipizide

Generic: glipizide

Labeler: northwind health company, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name glipizide
Generic Name glipizide
Labeler northwind health company, llc
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

glipizide 5 mg/1

Manufacturer
Northwind Health Company, LLC

Identifiers & Regulatory

Product NDC 82868-025
Product ID 82868-025_46dc8f32-692a-a243-e063-6394a90a19f8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206928
Listing Expiration 2026-12-31
Marketing Start 2023-11-08

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82868025
Hyphenated Format 82868-025

Supplemental Identifiers

RxCUI
314006
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 ANDA206928 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-025-30)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-025-90)
source: ndc

Packages (2)

82868-025-30 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-025-30) 82868-025-90 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-025-90)

Ingredients (1)

glipizide (5 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": "46dc8f32-692a-a243-e063-6394a90a19f8", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["X7WDT95N5C"], "rxcui": ["314006"], "spl_set_id": ["0a1e1152-ade7-2092-e063-6394a90a99e7"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-025-30)", "package_ndc": "82868-025-30", "marketing_start_date": "20240103"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-025-90)", "package_ndc": "82868-025-90", "marketing_start_date": "20231108"}], "brand_name": "Glipizide", "product_id": "82868-025_46dc8f32-692a-a243-e063-6394a90a19f8", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "82868-025", "generic_name": "Glipizide", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glipizide", "active_ingredients": [{"name": "GLIPIZIDE", "strength": "5 mg/1"}], "application_number": "ANDA206928", "marketing_category": "ANDA", "marketing_start_date": "20231108", "listing_expiration_date": "20261231"}