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, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

glipizide 10 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6848
Product ID 50090-6848_4edee9b0-23a0-4e64-a8c1-3dd89d5674cd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203499
Listing Expiration 2026-12-31
Marketing Start 2018-12-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500906848
Hyphenated Format 50090-6848

Supplemental Identifiers

RxCUI
315107
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 ANDA203499 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6848-0)
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6848-1)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6848-2)
source: ndc

Packages (3)

50090-6848-0 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6848-0) 50090-6848-1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6848-1) 50090-6848-2 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6848-2)

Ingredients (1)

glipizide (10 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": "4edee9b0-23a0-4e64-a8c1-3dd89d5674cd", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["X7WDT95N5C"], "rxcui": ["315107"], "spl_set_id": ["5014a2d7-e0d3-4e84-9a3e-c90b398b8c6c"], "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, EXTENDED RELEASE in 1 BOTTLE (50090-6848-0)", "package_ndc": "50090-6848-0", "marketing_start_date": "20231129"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6848-1)", "package_ndc": "50090-6848-1", "marketing_start_date": "20231129"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6848-2)", "package_ndc": "50090-6848-2", "marketing_start_date": "20231129"}], "brand_name": "Glipizide", "product_id": "50090-6848_4edee9b0-23a0-4e64-a8c1-3dd89d5674cd", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "50090-6848", "generic_name": "Glipizide", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glipizide", "active_ingredients": [{"name": "GLIPIZIDE", "strength": "10 mg/1"}], "application_number": "ANDA203499", "marketing_category": "ANDA", "marketing_start_date": "20181201", "listing_expiration_date": "20261231"}