Package 43063-122-90

Brand: glimepiride

Generic: glimepiride
NDC Package

Package Facts

Identity

Package NDC 43063-122-90
Digits Only 4306312290
Product NDC 43063-122
Product ID 43063-122_41372f7a-4296-6e3d-e063-6394a90af659
Description

90 TABLET in 1 BOTTLE, PLASTIC (43063-122-90)

Marketing

Marketing Status
Marketed Since 2009-12-23
Brand glimepiride
Generic glimepiride
Sample Package No

Linked Drug Pages (1)

Glimepiride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "41372f7a-4296-6e3d-e063-6394a90af659", "openfda": {"nui": ["N0000175608", "M0020795"], "upc": ["0343063122907"], "unii": ["6KY687524K"], "rxcui": ["199247"], "spl_set_id": ["101cdc41-2131-4425-b550-6a0a60b5f4a4"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-122-30)", "package_ndc": "43063-122-30", "marketing_start_date": "20241219"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (43063-122-90)", "package_ndc": "43063-122-90", "marketing_start_date": "20091223"}], "brand_name": "Glimepiride", "product_id": "43063-122_41372f7a-4296-6e3d-e063-6394a90af659", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "43063-122", "generic_name": "Glimepiride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glimepiride", "active_ingredients": [{"name": "GLIMEPIRIDE", "strength": "4 mg/1"}], "application_number": "ANDA077091", "marketing_category": "ANDA", "marketing_start_date": "20051006", "listing_expiration_date": "20261231"}