Package 72189-070-90

Brand: glipizide er

Generic: glipizide
NDC Package

Package Facts

Identity

Package NDC 72189-070-90
Digits Only 7218907090
Product NDC 72189-070
Product ID 72189-070_2be81315-9d2f-1301-e063-6394a90a6a84
Description

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

Marketing

Marketing Status
Marketed Since 2020-06-15
Brand glipizide er
Generic glipizide
Sample Package No

Linked Drug Pages (1)

GLIPIZIDE ER ndc-match (0.95)

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"}