glyburide

Generic: glyburide

Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name glyburide
Generic Name glyburide
Labeler heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

glyburide 2.5 mg/1

Manufacturer
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 23155-057
Product ID 23155-057_98ed9f46-1633-4f82-bd51-ff87b0157871
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 23155057
Hyphenated Format 23155-057

Supplemental Identifiers

RxCUI
197737 310534 310537
UPC
0323155056105 0323155058109 0323155057102 0323155058017 0323155057010 0323155056013
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 ANDA090937 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (23155-057-01)
  • 1000 TABLET in 1 BOTTLE (23155-057-10)
source: ndc

Packages (2)

23155-057-01 100 TABLET in 1 BOTTLE (23155-057-01) 23155-057-10 1000 TABLET in 1 BOTTLE (23155-057-10)

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": "98ed9f46-1633-4f82-bd51-ff87b0157871", "openfda": {"nui": ["N0000175608", "M0020795"], "upc": ["0323155056105", "0323155058109", "0323155057102", "0323155058017", "0323155057010", "0323155056013"], "unii": ["SX6K58TVWC"], "rxcui": ["197737", "310534", "310537"], "spl_set_id": ["33418bba-c5ea-4c0f-9d28-31dc2724c6c3"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (23155-057-01)", "package_ndc": "23155-057-01", "marketing_start_date": "20101005"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (23155-057-10)", "package_ndc": "23155-057-10", "marketing_start_date": "20101005"}], "brand_name": "GLYBURIDE", "product_id": "23155-057_98ed9f46-1633-4f82-bd51-ff87b0157871", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "23155-057", "generic_name": "GLYBURIDE", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "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"}