Package 71335-0069-1

Brand: glyburide

Generic: glyburide
NDC Package

Package Facts

Identity

Package NDC 71335-0069-1
Digits Only 7133500691
Product NDC 71335-0069
Description

30 TABLET in 1 BOTTLE (71335-0069-1)

Marketing

Marketing Status
Marketed Since 2018-11-08
Brand glyburide
Generic glyburide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "69d5da25-11fa-4522-84ee-d66a0a4dc4b5", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["SX6K58TVWC"], "rxcui": ["310534"], "spl_set_id": ["9cdd30e7-512a-4f00-a4de-0a154d143ce9"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-0069-1)", "package_ndc": "71335-0069-1", "marketing_start_date": "20181108"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-0069-2)", "package_ndc": "71335-0069-2", "marketing_start_date": "20250128"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-0069-3)", "package_ndc": "71335-0069-3", "marketing_start_date": "20191120"}], "brand_name": "GLYBURIDE", "product_id": "71335-0069_69d5da25-11fa-4522-84ee-d66a0a4dc4b5", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "71335-0069", "generic_name": "GLYBURIDE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "GLYBURIDE", "active_ingredients": [{"name": "GLYBURIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA090937", "marketing_category": "ANDA", "marketing_start_date": "20101005", "listing_expiration_date": "20261231"}