glipizide and metformin hcl

Generic: glipizide and metformin hcl

Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name glipizide and metformin hcl
Generic Name glipizide and metformin hcl
Labeler heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

glipizide 2.5 mg/1, metformin hydrochloride 500 mg/1

Manufacturer
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 23155-116
Product ID 23155-116_f6a0152a-4cab-48f9-b14c-31c662f676ed
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078728
Listing Expiration 2026-12-31
Marketing Start 2010-06-29

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 23155116
Hyphenated Format 23155-116

Supplemental Identifiers

RxCUI
861731 861736 861740
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 hcl (source: ndc)
Generic Name glipizide and metformin hcl (source: ndc)
Application Number ANDA078728 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
  • 500 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (23155-116-01)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (23155-116-10)
source: ndc

Packages (2)

Ingredients (2)

glipizide (2.5 mg/1) metformin hydrochloride (500 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f6a0152a-4cab-48f9-b14c-31c662f676ed", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["X7WDT95N5C", "786Z46389E"], "rxcui": ["861731", "861736", "861740"], "spl_set_id": ["94a7f96e-2ed1-432d-bc6a-5840863816e1"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (23155-116-01)", "package_ndc": "23155-116-01", "marketing_start_date": "20100629"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (23155-116-10)", "package_ndc": "23155-116-10", "marketing_start_date": "20100629"}], "brand_name": "Glipizide and Metformin HCl", "product_id": "23155-116_f6a0152a-4cab-48f9-b14c-31c662f676ed", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]", "Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "23155-116", "generic_name": "Glipizide and Metformin HCl", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glipizide and Metformin HCl", "active_ingredients": [{"name": "GLIPIZIDE", "strength": "2.5 mg/1"}, {"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA078728", "marketing_category": "ANDA", "marketing_start_date": "20100629", "listing_expiration_date": "20261231"}