glipizide
Generic: glipizide
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
glipizide
Generic Name
glipizide
Labeler
bryant ranch prepack
Dosage Form
TABLET, FILM COATED, EXTENDED RELEASE
Routes
Active Ingredients
glipizide 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-1130
Product ID
71335-1130_b2e42e92-1292-4d1e-b235-6e252e708b1c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA204720
Listing Expiration
2026-12-31
Marketing Start
2017-04-24
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713351130
Hyphenated Format
71335-1130
Supplemental Identifiers
RxCUI
UNII
NUI
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
ANDA204720 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1130-1)
- 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1130-2)
- 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1130-3)
- 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1130-4)
- 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1130-5)
Packages (5)
71335-1130-1
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1130-1)
71335-1130-2
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1130-2)
71335-1130-3
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1130-3)
71335-1130-4
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1130-4)
71335-1130-5
180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1130-5)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b2e42e92-1292-4d1e-b235-6e252e708b1c", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["X7WDT95N5C"], "rxcui": ["310489", "314006", "315107"], "spl_set_id": ["0338aff9-29f9-405e-b516-06ef4b863863"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1130-1)", "package_ndc": "71335-1130-1", "marketing_start_date": "20190306"}, {"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1130-2)", "package_ndc": "71335-1130-2", "marketing_start_date": "20190306"}, {"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1130-3)", "package_ndc": "71335-1130-3", "marketing_start_date": "20190306"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1130-4)", "package_ndc": "71335-1130-4", "marketing_start_date": "20190306"}, {"sample": false, "description": "180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1130-5)", "package_ndc": "71335-1130-5", "marketing_start_date": "20190306"}], "brand_name": "Glipizide", "product_id": "71335-1130_b2e42e92-1292-4d1e-b235-6e252e708b1c", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "71335-1130", "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": "ANDA204720", "marketing_category": "ANDA", "marketing_start_date": "20170424", "listing_expiration_date": "20261231"}