Package 72336-641-01
Brand: glimepiride 3 mg
Generic: glimepiridePackage Facts
Identity
Package NDC
72336-641-01
Digits Only
7233664101
Product NDC
72336-641
Description
100 TABLET in 1 BOTTLE (72336-641-01)
Marketing
Marketing Status
Brand
glimepiride 3 mg
Generic
glimepiride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8f56950f-d08d-44d4-9c7c-9830e9bfadb8", "openfda": {"nui": ["N0000175608", "M0020795"], "upc": ["0372336641012"], "unii": ["6KY687524K"], "rxcui": ["153842"], "spl_set_id": ["51157849-7990-4a8b-ae50-eda1baf93cfa"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Lifsa Drugs LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72336-641-01)", "package_ndc": "72336-641-01", "marketing_start_date": "20240820"}], "brand_name": "Glimepiride 3 mg", "product_id": "72336-641_8f56950f-d08d-44d4-9c7c-9830e9bfadb8", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "72336-641", "generic_name": "Glimepiride", "labeler_name": "Lifsa Drugs LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glimepiride 3 mg", "active_ingredients": [{"name": "GLIMEPIRIDE", "strength": "3 mg/1"}], "application_number": "ANDA091220", "marketing_category": "ANDA", "marketing_start_date": "20240820", "listing_expiration_date": "20261231"}