glipizide

Generic: glipizide

Labeler: northwind health company, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name glipizide
Generic Name glipizide
Labeler northwind health company, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

glipizide 5 mg/1

Manufacturer
Northwind Health Company, LLC

Identifiers & Regulatory

Product NDC 51655-180
Product ID 51655-180_48c42223-ff56-f7b4-e063-6294a90a9284
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075795
Listing Expiration 2027-12-31
Marketing Start 2020-06-04

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51655180
Hyphenated Format 51655-180

Supplemental Identifiers

RxCUI
310490
UNII
X7WDT95N5C
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 glipizide (source: ndc)
Generic Name glipizide (source: ndc)
Application Number ANDA075795 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 60 TABLET in 1 BOTTLE, PLASTIC (51655-180-25)
  • 90 TABLET in 1 BOTTLE, PLASTIC (51655-180-26)
  • 30 TABLET in 1 BOTTLE, PLASTIC (51655-180-52)
source: ndc

Packages (3)

51655-180-25 60 TABLET in 1 BOTTLE, PLASTIC (51655-180-25) 51655-180-26 90 TABLET in 1 BOTTLE, PLASTIC (51655-180-26) 51655-180-52 30 TABLET in 1 BOTTLE, PLASTIC (51655-180-52)

Ingredients (1)

glipizide (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": "48c42223-ff56-f7b4-e063-6294a90a9284", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["X7WDT95N5C"], "rxcui": ["310490"], "spl_set_id": ["c16edad6-4271-6ff0-e053-2a95a90a0240"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (51655-180-25)", "package_ndc": "51655-180-25", "marketing_start_date": "20221205"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (51655-180-26)", "package_ndc": "51655-180-26", "marketing_start_date": "20200604"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-180-52)", "package_ndc": "51655-180-52", "marketing_start_date": "20220330"}], "brand_name": "Glipizide", "product_id": "51655-180_48c42223-ff56-f7b4-e063-6294a90a9284", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "51655-180", "generic_name": "Glipizide", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glipizide", "active_ingredients": [{"name": "GLIPIZIDE", "strength": "5 mg/1"}], "application_number": "ANDA075795", "marketing_category": "ANDA", "marketing_start_date": "20200604", "listing_expiration_date": "20271231"}