Package 60760-800-90
Brand: glimepiride
Generic: glimepiridePackage Facts
Identity
Package NDC
60760-800-90
Digits Only
6076080090
Product NDC
60760-800
Description
90 TABLET in 1 BOTTLE, PLASTIC (60760-800-90)
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": "fc9df15f-22a5-f7a1-e053-6294a90a5b6d", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["6KY687524K"], "rxcui": ["199247"], "spl_set_id": ["fc9d8495-184c-3af1-e053-6394a90a5e29"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (60760-800-90)", "package_ndc": "60760-800-90", "marketing_start_date": "20230519"}], "brand_name": "Glimepiride", "product_id": "60760-800_fc9df15f-22a5-f7a1-e053-6294a90a5b6d", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "60760-800", "generic_name": "Glimepiride", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glimepiride", "active_ingredients": [{"name": "GLIMEPIRIDE", "strength": "4 mg/1"}], "application_number": "ANDA202759", "marketing_category": "ANDA", "marketing_start_date": "20230519", "listing_expiration_date": "20261231"}