glipizide

Generic: glipizide

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name glipizide
Generic Name glipizide
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

glipizide 10 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-2102
Product ID 72162-2102_728036ca-06bb-4034-b9a3-77b4b26f0e6f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075795
Listing Expiration 2026-12-31
Marketing Start 2002-09-25

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 721622102
Hyphenated Format 72162-2102

Supplemental Identifiers

RxCUI
310488
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 ANDA075795 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE (72162-2102-0)
source: ndc

Packages (1)

72162-2102-0 1000 TABLET in 1 BOTTLE (72162-2102-0)

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": "728036ca-06bb-4034-b9a3-77b4b26f0e6f", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["X7WDT95N5C"], "rxcui": ["310488"], "spl_set_id": ["be20727f-2724-457a-89ac-aa96604a0015"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (72162-2102-0)", "package_ndc": "72162-2102-0", "marketing_start_date": "20020925"}], "brand_name": "Glipizide", "product_id": "72162-2102_728036ca-06bb-4034-b9a3-77b4b26f0e6f", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "72162-2102", "generic_name": "Glipizide", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glipizide", "active_ingredients": [{"name": "GLIPIZIDE", "strength": "10 mg/1"}], "application_number": "ANDA075795", "marketing_category": "ANDA", "marketing_start_date": "20020925", "listing_expiration_date": "20261231"}