Package 68645-566-90
Brand: lovastatin
Generic: lovastatinPackage Facts
Identity
Package NDC
68645-566-90
Digits Only
6864556690
Product NDC
68645-566
Description
90 TABLET in 1 BOTTLE (68645-566-90)
Marketing
Marketing Status
Brand
lovastatin
Generic
lovastatin
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4cc241a1-d876-0439-e063-6394a90a2733", "openfda": {"nui": ["N0000175589", "N0000000121"], "upc": ["0368645566900", "0368645567907"], "unii": ["9LHU78OQFD"], "spl_set_id": ["a4f02fa1-3281-46fa-bd52-323e2644b6f8"], "pharm_class_epc": ["HMG-CoA Reductase Inhibitor [EPC]"], "pharm_class_moa": ["Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "manufacturer_name": ["Legacy Pharmaceutical Packaging, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (68645-566-90)", "package_ndc": "68645-566-90", "marketing_start_date": "20071101"}], "brand_name": "Lovastatin", "product_id": "68645-566_4cc241a1-d876-0439-e063-6394a90a2733", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "68645-566", "generic_name": "lovastatin", "labeler_name": "Legacy Pharmaceutical Packaging, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lovastatin", "active_ingredients": [{"name": "LOVASTATIN", "strength": "20 mg/1"}], "application_number": "ANDA078296", "marketing_category": "ANDA", "marketing_start_date": "20071101", "listing_expiration_date": "20271231"}