glipizide

Generic: glipizide

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name glipizide
Generic Name glipizide
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

glipizide 5 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7755
Product ID 50090-7755_0cb552e8-9478-4664-b1eb-9b0ae4ce48cc
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214874
Listing Expiration 2026-12-31
Marketing Start 2023-10-03

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907755
Hyphenated Format 50090-7755

Supplemental Identifiers

RxCUI
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 ANDA214874 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (50090-7755-0)
  • 60 TABLET in 1 BOTTLE (50090-7755-1)
  • 100 TABLET in 1 BOTTLE (50090-7755-2)
  • 90 TABLET in 1 BOTTLE (50090-7755-3)
  • 180 TABLET in 1 BOTTLE (50090-7755-4)
source: ndc

Packages (5)

Ingredients (1)

glipizide (5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0cb552e8-9478-4664-b1eb-9b0ae4ce48cc", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["X7WDT95N5C"], "rxcui": ["310490"], "spl_set_id": ["69a21bd3-3364-4035-b098-3808cc8cf8b2"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-7755-0)", "package_ndc": "50090-7755-0", "marketing_start_date": "20251105"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-7755-1)", "package_ndc": "50090-7755-1", "marketing_start_date": "20251105"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (50090-7755-2)", "package_ndc": "50090-7755-2", "marketing_start_date": "20251105"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7755-3)", "package_ndc": "50090-7755-3", "marketing_start_date": "20251105"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (50090-7755-4)", "package_ndc": "50090-7755-4", "marketing_start_date": "20251105"}], "brand_name": "Glipizide", "product_id": "50090-7755_0cb552e8-9478-4664-b1eb-9b0ae4ce48cc", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "50090-7755", "generic_name": "Glipizide", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glipizide", "active_ingredients": [{"name": "GLIPIZIDE", "strength": "5 mg/1"}], "application_number": "ANDA214874", "marketing_category": "ANDA", "marketing_start_date": "20231003", "listing_expiration_date": "20261231"}