Package 43063-946-93

Brand: glimepiride

Generic: glimepiride
NDC Package

Package Facts

Identity

Package NDC 43063-946-93
Digits Only 4306394693
Product NDC 43063-946
Description

180 TABLET in 1 BOTTLE, PLASTIC (43063-946-93)

Marketing

Marketing Status
Marketed Since 2023-01-18
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": "2ad37443-418f-0526-e063-6394a90a4e31", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["6KY687524K"], "rxcui": ["199246"], "spl_set_id": ["2794f86b-d521-414b-8154-5dd1e2519653"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET in 1 BOTTLE, PLASTIC (43063-946-93)", "package_ndc": "43063-946-93", "marketing_start_date": "20230118"}], "brand_name": "Glimepiride", "product_id": "43063-946_2ad37443-418f-0526-e063-6394a90a4e31", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "43063-946", "generic_name": "Glimepiride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glimepiride", "active_ingredients": [{"name": "GLIMEPIRIDE", "strength": "2 mg/1"}], "application_number": "ANDA077911", "marketing_category": "ANDA", "marketing_start_date": "20120101", "listing_expiration_date": "20261231"}