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 82804-959
Product ID 82804-959_f5d7a98c-d1d4-43b9-8d7e-830a33ae0c24
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074378
Listing Expiration 2027-12-31
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 82804959
Hyphenated Format 82804-959

Supplemental Identifiers

RxCUI
310488 310490
UPC
0382804960309 0382804959303
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 ANDA074378 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (82804-959-00)
  • 1000 TABLET in 1 BOTTLE (82804-959-11)
  • 30 TABLET in 1 BOTTLE (82804-959-30)
  • 500 TABLET in 1 BOTTLE (82804-959-55)
  • 60 TABLET in 1 BOTTLE (82804-959-60)
  • 120 TABLET in 1 BOTTLE (82804-959-72)
  • 90 TABLET in 1 BOTTLE (82804-959-90)
source: ndc

Packages (7)

82804-959-00 100 TABLET in 1 BOTTLE (82804-959-00) 82804-959-11 1000 TABLET in 1 BOTTLE (82804-959-11) 82804-959-30 30 TABLET in 1 BOTTLE (82804-959-30) 82804-959-55 500 TABLET in 1 BOTTLE (82804-959-55) 82804-959-60 60 TABLET in 1 BOTTLE (82804-959-60) 82804-959-72 120 TABLET in 1 BOTTLE (82804-959-72) 82804-959-90 90 TABLET in 1 BOTTLE (82804-959-90)

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": "f5d7a98c-d1d4-43b9-8d7e-830a33ae0c24", "openfda": {"nui": ["N0000175608", "M0020795"], "upc": ["0382804960309", "0382804959303"], "unii": ["X7WDT95N5C"], "rxcui": ["310488", "310490"], "spl_set_id": ["f5d7a98c-d1d4-43b9-8d7e-830a33ae0c24"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (82804-959-00)", "package_ndc": "82804-959-00", "marketing_start_date": "20260112"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (82804-959-11)", "package_ndc": "82804-959-11", "marketing_start_date": "20260112"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (82804-959-30)", "package_ndc": "82804-959-30", "marketing_start_date": "20260112"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (82804-959-55)", "package_ndc": "82804-959-55", "marketing_start_date": "20260112"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (82804-959-60)", "package_ndc": "82804-959-60", "marketing_start_date": "20260112"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (82804-959-72)", "package_ndc": "82804-959-72", "marketing_start_date": "20260112"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (82804-959-90)", "package_ndc": "82804-959-90", "marketing_start_date": "20260112"}], "brand_name": "Glipizide", "product_id": "82804-959_f5d7a98c-d1d4-43b9-8d7e-830a33ae0c24", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "82804-959", "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": "ANDA074378", "marketing_category": "ANDA", "marketing_start_date": "20250501", "listing_expiration_date": "20271231"}