glipizide

Generic: glipizide

Labeler: trupharma llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name glipizide
Generic Name glipizide
Labeler trupharma llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

glipizide 2.5 mg/1

Manufacturer
TruPharma LLC

Identifiers & Regulatory

Product NDC 52817-385
Product ID 52817-385_076b74ec-ead5-781c-e063-6394a90ab362
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214874
Listing Expiration 2026-12-31
Marketing Start 2023-10-03

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 52817385
Hyphenated Format 52817-385

Supplemental Identifiers

RxCUI
379804
UPC
0352817385109 0352817385505
UNII
X7WDT95N5C
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 glipizide (source: ndc)
Generic Name glipizide (source: ndc)
Application Number ANDA214874 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (52817-385-10)
  • 500 TABLET in 1 BOTTLE (52817-385-50)
source: ndc

Packages (2)

52817-385-10 100 TABLET in 1 BOTTLE (52817-385-10) 52817-385-50 500 TABLET in 1 BOTTLE (52817-385-50)

Ingredients (1)

glipizide (2.5 mg/1)

Linked Drug Pages (1)

Glipizide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "076b74ec-ead5-781c-e063-6394a90ab362", "openfda": {"nui": ["N0000175608", "M0020795"], "upc": ["0352817385109", "0352817385505"], "unii": ["X7WDT95N5C"], "rxcui": ["379804"], "spl_set_id": ["95ea4c96-84b9-4515-9494-a93d26820f70"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["TruPharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (52817-385-10)", "package_ndc": "52817-385-10", "marketing_start_date": "20231003"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (52817-385-50)", "package_ndc": "52817-385-50", "marketing_start_date": "20231003"}], "brand_name": "Glipizide", "product_id": "52817-385_076b74ec-ead5-781c-e063-6394a90ab362", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "52817-385", "generic_name": "Glipizide", "labeler_name": "TruPharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glipizide", "active_ingredients": [{"name": "GLIPIZIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA214874", "marketing_category": "ANDA", "marketing_start_date": "20231003", "listing_expiration_date": "20261231"}