glipizide and metformin hcl
Generic: glipizide and metformin hcl
Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.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
Active Ingredients
glipizide 2.5 mg/1, metformin hydrochloride 500 mg/1
Manufacturer
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)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
23155116
Hyphenated Format
23155-116
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 2.5 mg/1
- 500 mg/1
Packaging
- 100 TABLET, FILM COATED in 1 BOTTLE (23155-116-01)
- 1000 TABLET, FILM COATED in 1 BOTTLE (23155-116-10)
Packages (2)
Ingredients (2)
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"}