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, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

glipizide 5 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-9742
Product ID 71335-9742_9ed306fc-4226-4b04-a733-8db55ba4ebb8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206928
Listing Expiration 2026-12-31
Marketing Start 2023-03-03

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713359742
Hyphenated Format 71335-9742

Supplemental Identifiers

RxCUI
314006
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 ANDA206928 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9742-1)
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9742-2)
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9742-3)
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9742-4)
source: ndc

Packages (4)

71335-9742-1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9742-1) 71335-9742-2 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9742-2) 71335-9742-3 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9742-3) 71335-9742-4 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9742-4)

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": "9ed306fc-4226-4b04-a733-8db55ba4ebb8", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["X7WDT95N5C"], "rxcui": ["314006"], "spl_set_id": ["4afa67b2-7f86-4189-93a5-6a605f74540d"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9742-1)", "package_ndc": "71335-9742-1", "marketing_start_date": "20230710"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9742-2)", "package_ndc": "71335-9742-2", "marketing_start_date": "20230710"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9742-3)", "package_ndc": "71335-9742-3", "marketing_start_date": "20230710"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9742-4)", "package_ndc": "71335-9742-4", "marketing_start_date": "20230710"}], "brand_name": "Glipizide", "product_id": "71335-9742_9ed306fc-4226-4b04-a733-8db55ba4ebb8", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "71335-9742", "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": "ANDA206928", "marketing_category": "ANDA", "marketing_start_date": "20230303", "listing_expiration_date": "20261231"}