glipizide and metformin hydrochloride

Generic: glipizide and metformin hydrochloride

Labeler: teva pharmaceuticals usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name glipizide and metformin hydrochloride
Generic Name glipizide and metformin hydrochloride
Labeler teva pharmaceuticals usa, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

glipizide 5 mg/1, metformin hydrochloride 500 mg/1

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0093-7457
Product ID 0093-7457_50580ebe-be6b-439b-a39d-6536b9125fc1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077270
Listing Expiration 2026-12-31
Marketing Start 2005-10-28

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00937457
Hyphenated Format 0093-7457

Supplemental Identifiers

RxCUI
861731 861736 861740
UPC
0300937456018 0300937457015 0300937455011
UNII
X7WDT95N5C 786Z46389E
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 and metformin hydrochloride (source: ndc)
Generic Name glipizide and metformin hydrochloride (source: ndc)
Application Number ANDA077270 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
  • 500 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (0093-7457-01)
source: ndc

Packages (1)

0093-7457-01 100 TABLET, FILM COATED in 1 BOTTLE (0093-7457-01)

Ingredients (2)

glipizide (5 mg/1) metformin hydrochloride (500 mg/1)

Linked Drug Pages (1)

Glipizide and Metformin Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "50580ebe-be6b-439b-a39d-6536b9125fc1", "openfda": {"nui": ["N0000175608", "M0020795"], "upc": ["0300937456018", "0300937457015", "0300937455011"], "unii": ["X7WDT95N5C", "786Z46389E"], "rxcui": ["861731", "861736", "861740"], "spl_set_id": ["03d9ce02-0559-494c-a53d-de9b9a64b606"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0093-7457-01)", "package_ndc": "0093-7457-01", "marketing_start_date": "20051028"}], "brand_name": "Glipizide and Metformin Hydrochloride", "product_id": "0093-7457_50580ebe-be6b-439b-a39d-6536b9125fc1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]", "Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "0093-7457", "generic_name": "Glipizide and Metformin Hydrochloride", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glipizide and Metformin Hydrochloride", "active_ingredients": [{"name": "GLIPIZIDE", "strength": "5 mg/1"}, {"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA077270", "marketing_category": "ANDA", "marketing_start_date": "20051028", "listing_expiration_date": "20261231"}