glyburide

Generic: glyburide

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

Drug Facts

Product Profile

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

glyburide 5 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-0495
Product ID 50090-0495_d7312022-17ca-4251-a684-6045f7841266
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090937
Listing Expiration 2026-12-31
Marketing Start 2010-10-05

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500900495
Hyphenated Format 50090-0495

Supplemental Identifiers

RxCUI
310537
UNII
SX6K58TVWC
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 glyburide (source: ndc)
Generic Name glyburide (source: ndc)
Application Number ANDA090937 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (50090-0495-0)
  • 100 TABLET in 1 BOTTLE (50090-0495-1)
  • 60 TABLET in 1 BOTTLE (50090-0495-2)
  • 200 TABLET in 1 BOTTLE (50090-0495-8)
  • 90 TABLET in 1 BOTTLE (50090-0495-9)
source: ndc

Packages (5)

Ingredients (1)

glyburide (5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d7312022-17ca-4251-a684-6045f7841266", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["SX6K58TVWC"], "rxcui": ["310537"], "spl_set_id": ["3c91a408-973b-4572-832f-515f61d5be1f"], "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 (50090-0495-0)", "package_ndc": "50090-0495-0", "marketing_start_date": "20160629"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (50090-0495-1)", "package_ndc": "50090-0495-1", "marketing_start_date": "20160629"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-0495-2)", "package_ndc": "50090-0495-2", "marketing_start_date": "20160629"}, {"sample": false, "description": "200 TABLET in 1 BOTTLE (50090-0495-8)", "package_ndc": "50090-0495-8", "marketing_start_date": "20160629"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-0495-9)", "package_ndc": "50090-0495-9", "marketing_start_date": "20160629"}], "brand_name": "GLYBURIDE", "product_id": "50090-0495_d7312022-17ca-4251-a684-6045f7841266", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "50090-0495", "generic_name": "GLYBURIDE", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "GLYBURIDE", "active_ingredients": [{"name": "GLYBURIDE", "strength": "5 mg/1"}], "application_number": "ANDA090937", "marketing_category": "ANDA", "marketing_start_date": "20101005", "listing_expiration_date": "20261231"}