glipizide

Generic: glipizide

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

Drug Facts

Product Profile

Brand Name glipizide
Generic Name glipizide
Labeler aurobindo pharma limited
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

glipizide 10 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 59651-782
Product ID 59651-782_7d29a701-73cf-42ce-9068-b9a5153fdb56
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206928
Listing Expiration 2027-12-31
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 59651782
Hyphenated Format 59651-782

Supplemental Identifiers

RxCUI
310489 314006 315107
UPC
0359651782309 0359651781302
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 ANDA206928 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-782-01)
  • 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-782-05)
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-782-30)
  • 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-782-99)
source: ndc

Packages (4)

59651-782-01 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-782-01) 59651-782-05 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-782-05) 59651-782-30 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-782-30) 59651-782-99 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-782-99)

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": "7d29a701-73cf-42ce-9068-b9a5153fdb56", "openfda": {"nui": ["N0000175608", "M0020795"], "upc": ["0359651782309", "0359651781302"], "unii": ["X7WDT95N5C"], "rxcui": ["310489", "314006", "315107"], "spl_set_id": ["84794a52-b717-488c-8533-6425c83d405f"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-782-01)", "package_ndc": "59651-782-01", "marketing_start_date": "20230303"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-782-05)", "package_ndc": "59651-782-05", "marketing_start_date": "20230303"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-782-30)", "package_ndc": "59651-782-30", "marketing_start_date": "20230303"}, {"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-782-99)", "package_ndc": "59651-782-99", "marketing_start_date": "20230303"}], "brand_name": "Glipizide", "product_id": "59651-782_7d29a701-73cf-42ce-9068-b9a5153fdb56", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "59651-782", "generic_name": "Glipizide", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glipizide", "active_ingredients": [{"name": "GLIPIZIDE", "strength": "10 mg/1"}], "application_number": "ANDA206928", "marketing_category": "ANDA", "marketing_start_date": "20230303", "listing_expiration_date": "20271231"}