Package 68071-4232-1

Brand: glipizide

Generic: glipizide
NDC Package

Package Facts

Identity

Package NDC 68071-4232-1
Digits Only 6807142321
Product NDC 68071-4232
Description

100 TABLET in 1 BOTTLE (68071-4232-1)

Marketing

Marketing Status
Marketed Since 2018-01-15
Brand glipizide
Generic glipizide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1a3c62e9-ab6e-2693-e063-6394a90a74f8", "openfda": {"nui": ["N0000175608", "M0020795"], "upc": ["0368071423211"], "unii": ["X7WDT95N5C"], "rxcui": ["310488"], "spl_set_id": ["62d569b8-bb34-0e06-e053-2a91aa0a2ae1"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68071-4232-1)", "package_ndc": "68071-4232-1", "marketing_start_date": "20180115"}], "brand_name": "Glipizide", "product_id": "68071-4232_1a3c62e9-ab6e-2693-e063-6394a90a74f8", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "68071-4232", "generic_name": "Glipizide", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glipizide", "active_ingredients": [{"name": "GLIPIZIDE", "strength": "10 mg/1"}], "application_number": "ANDA075795", "marketing_category": "ANDA", "marketing_start_date": "20020925", "listing_expiration_date": "20261231"}