glipizide

Generic: glipizide

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name glipizide
Generic Name glipizide
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

glipizide 5 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 82804-174
Product ID 82804-174_abe14fb1-e2fa-4c89-8007-fa4c18fd70a2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214874
Listing Expiration 2026-12-31
Marketing Start 2023-10-03

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82804174
Hyphenated Format 82804-174

Supplemental Identifiers

RxCUI
310490
UPC
0382804174300
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
  • 5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (82804-174-30)
  • 90 TABLET in 1 BOTTLE (82804-174-90)
source: ndc

Packages (2)

82804-174-30 30 TABLET in 1 BOTTLE (82804-174-30) 82804-174-90 90 TABLET in 1 BOTTLE (82804-174-90)

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": "abe14fb1-e2fa-4c89-8007-fa4c18fd70a2", "openfda": {"nui": ["N0000175608", "M0020795"], "upc": ["0382804174300"], "unii": ["X7WDT95N5C"], "rxcui": ["310490"], "spl_set_id": ["6427db20-6783-439f-8c2d-64d1a6fcb9fc"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (82804-174-30)", "package_ndc": "82804-174-30", "marketing_start_date": "20241212"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (82804-174-90)", "package_ndc": "82804-174-90", "marketing_start_date": "20250120"}], "brand_name": "Glipizide", "product_id": "82804-174_abe14fb1-e2fa-4c89-8007-fa4c18fd70a2", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "82804-174", "generic_name": "Glipizide", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glipizide", "active_ingredients": [{"name": "GLIPIZIDE", "strength": "5 mg/1"}], "application_number": "ANDA214874", "marketing_category": "ANDA", "marketing_start_date": "20231003", "listing_expiration_date": "20261231"}