glipizide and metformin hydrochloride (50090-2492)

Drug Facts

Product Profile

Brand Name glipizide and metformin hydrochloride

Generic Name glipizide and metformin hydrochloride

Labeler a-s medication solutions

Dosage Form TABLET, FILM COATED

Routes

ORAL

Active Ingredients

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

Manufacturer

A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-2492

Product ID 50090-2492_1e31e5b7-d6ba-401b-a3d5-c27ef03f90c7

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA078905

Listing Expiration 2027-12-31

Marketing Start 2016-05-05

Pharmacologic Class

Established (EPC)

sulfonylurea [epc]

Chemical Structure

sulfonylurea compounds [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500902492

Hyphenated Format 50090-2492

Supplemental Identifiers

RxCUI

861736 861740

UNII

X7WDT95N5C 786Z46389E

NUI

N0000175608 M0020795

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 ANDA078905 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

2.5 mg/1
500 mg/1

source: ndc

Packaging

180 TABLET, FILM COATED in 1 BOTTLE (50090-2492-0)

source: ndc

Packages (1)

50090-2492-0 180 TABLET, FILM COATED in 1 BOTTLE (50090-2492-0)

Ingredients (2)

glipizide (2.5 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": "1e31e5b7-d6ba-401b-a3d5-c27ef03f90c7", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["X7WDT95N5C", "786Z46389E"], "rxcui": ["861736", "861740"], "spl_set_id": ["4a2d814b-93a1-4487-b789-dbafe9f0ffd3"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (50090-2492-0)", "package_ndc": "50090-2492-0", "marketing_start_date": "20161012"}], "brand_name": "Glipizide and Metformin Hydrochloride", "product_id": "50090-2492_1e31e5b7-d6ba-401b-a3d5-c27ef03f90c7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]", "Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "50090-2492", "generic_name": "Glipizide and Metformin Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glipizide and Metformin Hydrochloride", "active_ingredients": [{"name": "GLIPIZIDE", "strength": "2.5 mg/1"}, {"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA078905", "marketing_category": "ANDA", "marketing_start_date": "20160505", "listing_expiration_date": "20271231"}