glipizide er

Generic: glipizide

Labeler: direct rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name glipizide er
Generic Name glipizide
Labeler direct rx
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

glipizide 2.5 mg/1

Manufacturer
DIRECT RX

Identifiers & Regulatory

Product NDC 72189-070
Product ID 72189-070_2be81315-9d2f-1301-e063-6394a90a6a84
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076467
Listing Expiration 2026-12-31
Marketing Start 2020-06-15

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189070
Hyphenated Format 72189-070

Supplemental Identifiers

RxCUI
310489
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 er (source: ndc)
Generic Name glipizide (source: ndc)
Application Number ANDA076467 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72189-070-90)
source: ndc

Packages (1)

72189-070-90 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72189-070-90)

Ingredients (1)

glipizide (2.5 mg/1)

Linked Drug Pages (1)

GLIPIZIDE ER ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2be81315-9d2f-1301-e063-6394a90a6a84", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["X7WDT95N5C"], "rxcui": ["310489"], "spl_set_id": ["a825166c-fac2-06b1-e053-2995a90a58cf"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72189-070-90)", "package_ndc": "72189-070-90", "marketing_start_date": "20200615"}], "brand_name": "GLIPIZIDE ER", "product_id": "72189-070_2be81315-9d2f-1301-e063-6394a90a6a84", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "72189-070", "generic_name": "glipizide", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "GLIPIZIDE ER", "active_ingredients": [{"name": "GLIPIZIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA076467", "marketing_category": "ANDA", "marketing_start_date": "20200615", "listing_expiration_date": "20261231"}