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 5 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-2520
Product ID 71335-2520_997c3a0c-71a7-46b7-888a-a0e9c5152ec7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074497
Listing Expiration 2026-12-31
Marketing Start 2022-05-31

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713352520
Hyphenated Format 71335-2520

Supplemental Identifiers

RxCUI
310490
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 ANDA074497 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (71335-2520-1)
  • 30 TABLET in 1 BOTTLE (71335-2520-2)
  • 60 TABLET in 1 BOTTLE (71335-2520-3)
  • 90 TABLET in 1 BOTTLE (71335-2520-4)
  • 20 TABLET in 1 BOTTLE (71335-2520-5)
  • 180 TABLET in 1 BOTTLE (71335-2520-6)
  • 10 TABLET in 1 BOTTLE (71335-2520-7)
source: ndc

Packages (7)

71335-2520-1 100 TABLET in 1 BOTTLE (71335-2520-1) 71335-2520-2 30 TABLET in 1 BOTTLE (71335-2520-2) 71335-2520-3 60 TABLET in 1 BOTTLE (71335-2520-3) 71335-2520-4 90 TABLET in 1 BOTTLE (71335-2520-4) 71335-2520-5 20 TABLET in 1 BOTTLE (71335-2520-5) 71335-2520-6 180 TABLET in 1 BOTTLE (71335-2520-6) 71335-2520-7 10 TABLET in 1 BOTTLE (71335-2520-7)

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": "997c3a0c-71a7-46b7-888a-a0e9c5152ec7", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["X7WDT95N5C"], "rxcui": ["310490"], "spl_set_id": ["c0db4c38-6eed-49ca-84ab-7ed89e476822"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-2520-1)", "package_ndc": "71335-2520-1", "marketing_start_date": "20241104"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2520-2)", "package_ndc": "71335-2520-2", "marketing_start_date": "20241104"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-2520-3)", "package_ndc": "71335-2520-3", "marketing_start_date": "20241104"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2520-4)", "package_ndc": "71335-2520-4", "marketing_start_date": "20241104"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (71335-2520-5)", "package_ndc": "71335-2520-5", "marketing_start_date": "20241104"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71335-2520-6)", "package_ndc": "71335-2520-6", "marketing_start_date": "20241104"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (71335-2520-7)", "package_ndc": "71335-2520-7", "marketing_start_date": "20241104"}], "brand_name": "Glipizide", "product_id": "71335-2520_997c3a0c-71a7-46b7-888a-a0e9c5152ec7", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "71335-2520", "generic_name": "Glipizide", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glipizide", "active_ingredients": [{"name": "GLIPIZIDE", "strength": "5 mg/1"}], "application_number": "ANDA074497", "marketing_category": "ANDA", "marketing_start_date": "20220531", "listing_expiration_date": "20261231"}