glipizide

Generic: glipizide

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

Drug Facts

Product Profile

Brand Name glipizide
Generic Name glipizide
Labeler preferred pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

glipizide 5 mg/1

Manufacturer
Preferred Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68788-0141
Product ID 68788-0141_664464ef-39d9-49d9-81ea-c6f41d000ed5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075795
Listing Expiration 2026-12-31
Marketing Start 2013-02-18

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687880141
Hyphenated Format 68788-0141

Supplemental Identifiers

RxCUI
310488 310490
UNII
X7WDT95N5C
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 (source: ndc)
Generic Name glipizide (source: ndc)
Application Number ANDA075795 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (68788-0141-1)
  • 30 TABLET in 1 BOTTLE (68788-0141-3)
  • 60 TABLET in 1 BOTTLE (68788-0141-6)
  • 90 TABLET in 1 BOTTLE (68788-0141-9)
source: ndc

Packages (4)

68788-0141-1 100 TABLET in 1 BOTTLE (68788-0141-1) 68788-0141-3 30 TABLET in 1 BOTTLE (68788-0141-3) 68788-0141-6 60 TABLET in 1 BOTTLE (68788-0141-6) 68788-0141-9 90 TABLET in 1 BOTTLE (68788-0141-9)

Ingredients (1)

glipizide (5 mg/1)

Linked Drug Pages (1)

Glipizide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "664464ef-39d9-49d9-81ea-c6f41d000ed5", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["X7WDT95N5C"], "rxcui": ["310488", "310490"], "spl_set_id": ["097424ef-612f-4bc2-809a-e5bb8eeae244"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-0141-1)", "package_ndc": "68788-0141-1", "marketing_start_date": "20130218"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-0141-3)", "package_ndc": "68788-0141-3", "marketing_start_date": "20130218"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-0141-6)", "package_ndc": "68788-0141-6", "marketing_start_date": "20130218"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-0141-9)", "package_ndc": "68788-0141-9", "marketing_start_date": "20130218"}], "brand_name": "Glipizide", "product_id": "68788-0141_664464ef-39d9-49d9-81ea-c6f41d000ed5", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "68788-0141", "generic_name": "Glipizide", "labeler_name": "Preferred Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glipizide", "active_ingredients": [{"name": "GLIPIZIDE", "strength": "5 mg/1"}], "application_number": "ANDA075795", "marketing_category": "ANDA", "marketing_start_date": "20130218", "listing_expiration_date": "20261231"}