glipizide

Generic: glipizide

Labeler: advagen pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name glipizide
Generic Name glipizide
Labeler advagen pharma limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

glipizide 10 mg/1

Manufacturer
Advagen Pharma Limited

Identifiers & Regulatory

Product NDC 72888-117
Product ID 72888-117_4b92566f-0480-6f8a-e063-6394a90a53e0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214874
Listing Expiration 2027-12-31
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 72888117
Hyphenated Format 72888-117

Supplemental Identifiers

UPC
0372888117003 0372888116303 0372888231051 0372888231013 0372888117010 0372888117300 0372888115306 0372888116051 0372888116013 0372888115009 0372888115016 0372888116006 0372888117058 0372888115054 0372888231006
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 ANDA214874 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE (72888-117-00)
  • 100 TABLET in 1 BOTTLE (72888-117-01)
  • 500 TABLET in 1 BOTTLE (72888-117-05)
  • 30 TABLET in 1 BOTTLE (72888-117-30)
source: ndc

Packages (4)

72888-117-00 1000 TABLET in 1 BOTTLE (72888-117-00) 72888-117-01 100 TABLET in 1 BOTTLE (72888-117-01) 72888-117-05 500 TABLET in 1 BOTTLE (72888-117-05) 72888-117-30 30 TABLET in 1 BOTTLE (72888-117-30)

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": "4b92566f-0480-6f8a-e063-6394a90a53e0", "openfda": {"nui": ["N0000175608", "M0020795"], "upc": ["0372888117003", "0372888116303", "0372888231051", "0372888231013", "0372888117010", "0372888117300", "0372888115306", "0372888116051", "0372888116013", "0372888115009", "0372888115016", "0372888116006", "0372888117058", "0372888115054", "0372888231006"], "unii": ["X7WDT95N5C"], "spl_set_id": ["e954afb8-52eb-416a-8f1b-14b0fcb3bac2"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Advagen Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (72888-117-00)", "package_ndc": "72888-117-00", "marketing_start_date": "20231003"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (72888-117-01)", "package_ndc": "72888-117-01", "marketing_start_date": "20231003"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (72888-117-05)", "package_ndc": "72888-117-05", "marketing_start_date": "20231003"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (72888-117-30)", "package_ndc": "72888-117-30", "marketing_start_date": "20231003"}], "brand_name": "Glipizide", "product_id": "72888-117_4b92566f-0480-6f8a-e063-6394a90a53e0", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "72888-117", "generic_name": "Glipizide", "labeler_name": "Advagen Pharma Limited", "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": "20231003", "listing_expiration_date": "20271231"}