glipizide
Generic: glipizide
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
glipizide
Generic Name
glipizide
Labeler
a-s medication solutions
Dosage Form
TABLET
Routes
Active Ingredients
glipizide 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-7756
Product ID
50090-7756_8c7ab0b2-222d-45fc-acd2-d3cf8edc21e2
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)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500907756
Hyphenated Format
50090-7756
Supplemental Identifiers
RxCUI
UNII
NUI
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
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 90 TABLET in 1 BOTTLE (50090-7756-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8c7ab0b2-222d-45fc-acd2-d3cf8edc21e2", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["X7WDT95N5C"], "rxcui": ["310490"], "spl_set_id": ["c582d7d0-4db0-4296-8131-baefd1a671b2"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7756-0)", "package_ndc": "50090-7756-0", "marketing_start_date": "20251105"}], "brand_name": "Glipizide", "product_id": "50090-7756_8c7ab0b2-222d-45fc-acd2-d3cf8edc21e2", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "50090-7756", "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"}