Package 71610-709-45

Brand: lovastatin

Generic: lovastatin
NDC Package

Package Facts

Identity

Package NDC 71610-709-45
Digits Only 7161070945
Product NDC 71610-709
Description

45 TABLET in 1 BOTTLE (71610-709-45)

Marketing

Marketing Status
Marketed Since 2023-05-31
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": "20d6175b-0f94-4133-8b95-b8e3a4ef4139", "openfda": {"nui": ["N0000175589", "N0000000121"], "unii": ["9LHU78OQFD"], "rxcui": ["197905"], "spl_set_id": ["7e96b174-3887-4908-9b9f-5ef93540f96a"], "pharm_class_epc": ["HMG-CoA Reductase Inhibitor [EPC]"], "pharm_class_moa": ["Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "45 TABLET in 1 BOTTLE (71610-709-45)", "package_ndc": "71610-709-45", "marketing_start_date": "20230531"}], "brand_name": "Lovastatin", "product_id": "71610-709_20d6175b-0f94-4133-8b95-b8e3a4ef4139", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "71610-709", "generic_name": "Lovastatin", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lovastatin", "active_ingredients": [{"name": "LOVASTATIN", "strength": "40 mg/1"}], "application_number": "ANDA075551", "marketing_category": "ANDA", "marketing_start_date": "20011217", "listing_expiration_date": "20261231"}