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 2.5 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-5776
Product ID 50090-5776_e847f32b-6c85-4e8d-8733-3b0b850016eb
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 500905776
Hyphenated Format 50090-5776

Supplemental Identifiers

RxCUI
310534
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
  • 2.5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (50090-5776-0)
  • 200 TABLET in 1 BOTTLE (50090-5776-2)
source: ndc

Packages (2)

50090-5776-0 30 TABLET in 1 BOTTLE (50090-5776-0) 50090-5776-2 200 TABLET in 1 BOTTLE (50090-5776-2)

Ingredients (1)

glyburide (2.5 mg/1)

Linked Drug Pages (1)

GLYBURIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e847f32b-6c85-4e8d-8733-3b0b850016eb", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["SX6K58TVWC"], "rxcui": ["310534"], "spl_set_id": ["7a280f88-26d4-4fe5-a89b-a6f1d90ed3cd"], "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 (50090-5776-0)", "package_ndc": "50090-5776-0", "marketing_start_date": "20211007"}, {"sample": false, "description": "200 TABLET in 1 BOTTLE (50090-5776-2)", "package_ndc": "50090-5776-2", "marketing_start_date": "20211007"}], "brand_name": "GLYBURIDE", "product_id": "50090-5776_e847f32b-6c85-4e8d-8733-3b0b850016eb", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "50090-5776", "generic_name": "GLYBURIDE", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "GLYBURIDE", "active_ingredients": [{"name": "GLYBURIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA090937", "marketing_category": "ANDA", "marketing_start_date": "20101005", "listing_expiration_date": "20261231"}