glipizide

Generic: glipizide

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name glipizide
Generic Name glipizide
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

glipizide 5 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-130
Product ID 72789-130_4af77321-ff67-2bb7-e063-6394a90abecb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075795
Listing Expiration 2027-12-31
Marketing Start 2002-09-25

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72789130
Hyphenated Format 72789-130

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
  • 30 TABLET in 1 BOTTLE, PLASTIC (72789-130-30)
  • 90 TABLET in 1 BOTTLE, PLASTIC (72789-130-90)
source: ndc

Packages (2)

72789-130-30 30 TABLET in 1 BOTTLE, PLASTIC (72789-130-30) 72789-130-90 90 TABLET in 1 BOTTLE, PLASTIC (72789-130-90)

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": "4af77321-ff67-2bb7-e063-6394a90abecb", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["X7WDT95N5C"], "rxcui": ["310490"], "spl_set_id": ["f60b0690-aca9-40ec-956e-bd2ecc35ec54"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-130-30)", "package_ndc": "72789-130-30", "marketing_start_date": "20201123"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (72789-130-90)", "package_ndc": "72789-130-90", "marketing_start_date": "20201014"}], "brand_name": "Glipizide", "product_id": "72789-130_4af77321-ff67-2bb7-e063-6394a90abecb", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "72789-130", "generic_name": "Glipizide", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "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": "20020925", "listing_expiration_date": "20271231"}