glyburide

Generic: glyburide

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name glyburide
Generic Name glyburide
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

glyburide 2.5 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-0069
Product ID 71335-0069_69d5da25-11fa-4522-84ee-d66a0a4dc4b5
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 713350069
Hyphenated Format 71335-0069

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 (71335-0069-1)
  • 60 TABLET in 1 BOTTLE (71335-0069-2)
  • 90 TABLET in 1 BOTTLE (71335-0069-3)
source: ndc

Packages (3)

71335-0069-1 30 TABLET in 1 BOTTLE (71335-0069-1) 71335-0069-2 60 TABLET in 1 BOTTLE (71335-0069-2) 71335-0069-3 90 TABLET in 1 BOTTLE (71335-0069-3)

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": "69d5da25-11fa-4522-84ee-d66a0a4dc4b5", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["SX6K58TVWC"], "rxcui": ["310534"], "spl_set_id": ["9cdd30e7-512a-4f00-a4de-0a154d143ce9"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-0069-1)", "package_ndc": "71335-0069-1", "marketing_start_date": "20181108"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-0069-2)", "package_ndc": "71335-0069-2", "marketing_start_date": "20250128"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-0069-3)", "package_ndc": "71335-0069-3", "marketing_start_date": "20191120"}], "brand_name": "GLYBURIDE", "product_id": "71335-0069_69d5da25-11fa-4522-84ee-d66a0a4dc4b5", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "71335-0069", "generic_name": "GLYBURIDE", "labeler_name": "Bryant Ranch Prepack", "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"}