Package 50090-7407-0

Brand: glimepiride

Generic: glimepiride
NDC Package

Package Facts

Identity

Package NDC 50090-7407-0
Digits Only 5009074070
Product NDC 50090-7407
Description

90 TABLET in 1 BOTTLE (50090-7407-0)

Marketing

Marketing Status
Marketed Since 2024-10-24
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": "ab61e15d-47e6-43ab-b57b-d6493c2889ba", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["6KY687524K"], "rxcui": ["199247"], "spl_set_id": ["0c25c987-856f-448d-903a-e2c94049b0a7"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7407-0)", "package_ndc": "50090-7407-0", "marketing_start_date": "20241024"}], "brand_name": "Glimepiride", "product_id": "50090-7407_ab61e15d-47e6-43ab-b57b-d6493c2889ba", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "50090-7407", "generic_name": "Glimepiride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glimepiride", "active_ingredients": [{"name": "GLIMEPIRIDE", "strength": "4 mg/1"}], "application_number": "ANDA202112", "marketing_category": "ANDA", "marketing_start_date": "20230731", "listing_expiration_date": "20261231"}