glyburide

Generic: glyburide

Labeler: modavar pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name glyburide
Generic Name glyburide
Labeler modavar pharmaceuticals llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

glyburide 2.5 mg/1

Manufacturer
Modavar Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 72241-039
Product ID 72241-039_7ebf5b06-fdd3-4120-93f2-d31def5bf104
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203379
Listing Expiration 2026-12-31
Marketing Start 2021-10-05

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72241039
Hyphenated Format 72241-039

Supplemental Identifiers

RxCUI
197737 310534 310537
UPC
0372241039058 0372241040054 0372241038051
UNII
SX6K58TVWC
NUI
N0000175608 M0020795

Packaging Origin

Original Packager
true

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 ANDA203379 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (72241-039-05)
  • 500 TABLET in 1 BOTTLE (72241-039-10)
  • 1000 TABLET in 1 BOTTLE (72241-039-11)
source: ndc

Packages (3)

72241-039-05 100 TABLET in 1 BOTTLE (72241-039-05) 72241-039-10 500 TABLET in 1 BOTTLE (72241-039-10) 72241-039-11 1000 TABLET in 1 BOTTLE (72241-039-11)

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": "7ebf5b06-fdd3-4120-93f2-d31def5bf104", "openfda": {"nui": ["N0000175608", "M0020795"], "upc": ["0372241039058", "0372241040054", "0372241038051"], "unii": ["SX6K58TVWC"], "rxcui": ["197737", "310534", "310537"], "spl_set_id": ["a5de0ef6-4c8b-40ab-b0ed-2003a8086750"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Modavar Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72241-039-05)", "package_ndc": "72241-039-05", "marketing_start_date": "20211005"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (72241-039-10)", "package_ndc": "72241-039-10", "marketing_start_date": "20211005"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (72241-039-11)", "package_ndc": "72241-039-11", "marketing_start_date": "20211005"}], "brand_name": "Glyburide", "product_id": "72241-039_7ebf5b06-fdd3-4120-93f2-d31def5bf104", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "72241-039", "generic_name": "Glyburide", "labeler_name": "Modavar Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glyburide", "active_ingredients": [{"name": "GLYBURIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA203379", "marketing_category": "ANDA", "marketing_start_date": "20211005", "listing_expiration_date": "20261231"}