glyburide
Generic: glyburide
Labeler: nucare pharmaceuticals,inc.Drug Facts
Product Profile
Brand Name
glyburide
Generic Name
glyburide
Labeler
nucare pharmaceuticals,inc.
Dosage Form
TABLET
Routes
Active Ingredients
glyburide 2.5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68071-5217
Product ID
68071-5217_1b58e185-0bf6-c0eb-e063-6294a90a4d9f
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)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680715217
Hyphenated Format
68071-5217
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
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
source: ndc
Resolved Composition
Strengths
- 2.5 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (68071-5217-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1b58e185-0bf6-c0eb-e063-6294a90a4d9f", "openfda": {"nui": ["N0000175608", "M0020795"], "upc": ["0368071521702"], "unii": ["SX6K58TVWC"], "rxcui": ["310534"], "spl_set_id": ["a1233548-bbb8-34aa-e053-2a95a90aea53"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68071-5217-0)", "package_ndc": "68071-5217-0", "marketing_start_date": "20200318"}], "brand_name": "GLYBURIDE", "product_id": "68071-5217_1b58e185-0bf6-c0eb-e063-6294a90a4d9f", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "68071-5217", "generic_name": "GLYBURIDE", "labeler_name": "NuCare 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"}