glipizide and metformin hcl

Generic: glipizide and metformin hcl

Labeler: proficient rx lp
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 proficient rx lp
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

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

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-270
Product ID 71205-270_ba23a55b-30dd-4d55-a423-3542524a8efe
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 71205270
Hyphenated Format 71205-270

Supplemental Identifiers

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

Resolved Composition

Strengths
  • 5 mg/1
  • 500 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (71205-270-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71205-270-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71205-270-90)
source: ndc

Packages (3)

Ingredients (2)

glipizide (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": "ba23a55b-30dd-4d55-a423-3542524a8efe", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["X7WDT95N5C", "786Z46389E"], "rxcui": ["861740"], "spl_set_id": ["be4d2552-c964-4d09-ba7a-0d94320f968c"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-270-30)", "package_ndc": "71205-270-30", "marketing_start_date": "20190501"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-270-60)", "package_ndc": "71205-270-60", "marketing_start_date": "20190501"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-270-90)", "package_ndc": "71205-270-90", "marketing_start_date": "20190501"}], "brand_name": "Glipizide and Metformin HCl", "product_id": "71205-270_ba23a55b-30dd-4d55-a423-3542524a8efe", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]", "Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "71205-270", "generic_name": "Glipizide and Metformin HCl", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glipizide and Metformin HCl", "active_ingredients": [{"name": "GLIPIZIDE", "strength": "5 mg/1"}, {"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA078728", "marketing_category": "ANDA", "marketing_start_date": "20100629", "listing_expiration_date": "20261231"}