Package 43063-121-90
Brand: glimepiride
Generic: glimepiridePackage Facts
Identity
Package NDC
43063-121-90
Digits Only
4306312190
Product NDC
43063-121
Description
90 TABLET in 1 BOTTLE, PLASTIC (43063-121-90)
Marketing
Marketing Status
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": "4137398e-13df-7c18-e063-6394a90ac45d", "openfda": {"nui": ["N0000175608", "M0020795"], "upc": ["0343063121900"], "unii": ["6KY687524K"], "rxcui": ["199245"], "spl_set_id": ["657f1b51-2f82-44f6-a23d-97f4b34b3c45"], "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 (43063-121-30)", "package_ndc": "43063-121-30", "marketing_start_date": "20091223"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (43063-121-90)", "package_ndc": "43063-121-90", "marketing_start_date": "20091223"}], "brand_name": "Glimepiride", "product_id": "43063-121_4137398e-13df-7c18-e063-6394a90ac45d", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "43063-121", "generic_name": "Glimepiride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glimepiride", "active_ingredients": [{"name": "GLIMEPIRIDE", "strength": "1 mg/1"}], "application_number": "ANDA077091", "marketing_category": "ANDA", "marketing_start_date": "20051006", "listing_expiration_date": "20261231"}