Package 68788-8232-3
Brand: lovastatin
Generic: lovastatinPackage Facts
Identity
Package NDC
68788-8232-3
Digits Only
6878882323
Product NDC
68788-8232
Description
30 TABLET in 1 BOTTLE (68788-8232-3)
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": "19500b45-4a52-42a9-b3a5-36d634d4dd61", "openfda": {"nui": ["N0000175589", "N0000000121"], "unii": ["9LHU78OQFD"], "rxcui": ["197905"], "spl_set_id": ["397949f9-ce60-424f-9902-90e65a34f4de"], "pharm_class_epc": ["HMG-CoA Reductase Inhibitor [EPC]"], "pharm_class_moa": ["Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8232-3)", "package_ndc": "68788-8232-3", "marketing_start_date": "20220808"}], "brand_name": "Lovastatin", "product_id": "68788-8232_19500b45-4a52-42a9-b3a5-36d634d4dd61", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "68788-8232", "generic_name": "lovastatin", "labeler_name": "Preferred Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lovastatin", "active_ingredients": [{"name": "LOVASTATIN", "strength": "40 mg/1"}], "application_number": "ANDA078296", "marketing_category": "ANDA", "marketing_start_date": "20220808", "listing_expiration_date": "20261231"}