Package 48792-7865-1
Brand: linagliptin
Generic: linagliptinPackage Facts
Identity
Package NDC
48792-7865-1
Digits Only
4879278651
Product NDC
48792-7865
Description
30 TABLET, FILM COATED in 1 BOTTLE (48792-7865-1)
Marketing
Marketing Status
Brand
linagliptin
Generic
linagliptin
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4865a926-1da4-15be-e063-6294a90a4b76", "openfda": {"nui": ["N0000175912", "N0000175913"], "unii": ["3X29ZEJ4R2"], "rxcui": ["1100702"], "spl_set_id": ["cbdbd4b2-c07b-00e1-e053-2995a90a5fc9"], "pharm_class_epc": ["Dipeptidyl Peptidase 4 Inhibitor [EPC]"], "pharm_class_moa": ["Dipeptidyl Peptidase 4 Inhibitors [MoA]"], "manufacturer_name": ["Sunshine Lake Pharma Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (48792-7865-1)", "package_ndc": "48792-7865-1", "marketing_start_date": "20260101"}], "brand_name": "linagliptin", "product_id": "48792-7865_4865a926-1da4-15be-e063-6294a90a4b76", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Dipeptidyl Peptidase 4 Inhibitor [EPC]", "Dipeptidyl Peptidase 4 Inhibitors [MoA]"], "product_ndc": "48792-7865", "generic_name": "linagliptin", "labeler_name": "Sunshine Lake Pharma Co., Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "linagliptin", "active_ingredients": [{"name": "LINAGLIPTIN", "strength": "5 mg/1"}], "application_number": "ANDA208335", "marketing_category": "ANDA", "marketing_start_date": "20260101", "listing_expiration_date": "20271231"}