Package 71921-214-01

Brand: glimepiride

Generic: glimepiride
NDC Package

Package Facts

Identity

Package NDC 71921-214-01
Digits Only 7192121401
Product NDC 71921-214
Description

100 TABLET in 1 BOTTLE (71921-214-01)

Marketing

Marketing Status
Marketed Since 2023-07-31
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": "52fcdeaf-e64f-48bd-b90d-e7502b104ae1", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["6KY687524K"], "rxcui": ["199245", "199246", "199247"], "spl_set_id": ["8ff0de99-272e-4e68-9caf-69f3f146ac29"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Florida Pharmaceutical Products, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71921-214-01)", "package_ndc": "71921-214-01", "marketing_start_date": "20230731"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (71921-214-50)", "package_ndc": "71921-214-50", "marketing_start_date": "20230731"}], "brand_name": "Glimepiride", "product_id": "71921-214_52fcdeaf-e64f-48bd-b90d-e7502b104ae1", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "71921-214", "generic_name": "Glimepiride", "labeler_name": "Florida Pharmaceutical Products, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glimepiride", "active_ingredients": [{"name": "GLIMEPIRIDE", "strength": "1 mg/1"}], "application_number": "ANDA202112", "marketing_category": "ANDA", "marketing_start_date": "20230731", "listing_expiration_date": "20261231"}