Package 71205-779-90
Brand: glimepiride
Generic: glimepiridePackage Facts
Identity
Package NDC
71205-779-90
Digits Only
7120577990
Product NDC
71205-779
Description
90 TABLET in 1 BOTTLE (71205-779-90)
Marketing
Marketing Status
Brand
glimepiride
Generic
glimepiride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e12ab052-e3d6-4246-b727-f1e3f9057f09", "openfda": {"nui": ["N0000175608", "M0020795"], "upc": ["0371205779306"], "unii": ["6KY687524K"], "rxcui": ["199245"], "spl_set_id": ["e12ab052-e3d6-4246-b727-f1e3f9057f09"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-779-30)", "package_ndc": "71205-779-30", "marketing_start_date": "20230323"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-779-60)", "package_ndc": "71205-779-60", "marketing_start_date": "20230323"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-779-90)", "package_ndc": "71205-779-90", "marketing_start_date": "20230323"}], "brand_name": "Glimepiride", "product_id": "71205-779_e12ab052-e3d6-4246-b727-f1e3f9057f09", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "71205-779", "generic_name": "Glimepiride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glimepiride", "active_ingredients": [{"name": "GLIMEPIRIDE", "strength": "1 mg/1"}], "application_number": "ANDA202759", "marketing_category": "ANDA", "marketing_start_date": "20120629", "listing_expiration_date": "20261231"}