Package 71205-993-11
Brand: lovastatin
Generic: lovastatinPackage Facts
Identity
Package NDC
71205-993-11
Digits Only
7120599311
Product NDC
71205-993
Description
1000 TABLET in 1 BOTTLE (71205-993-11)
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": "e637904d-8af6-47fe-b10e-db813d5531bc", "openfda": {"nui": ["N0000175589", "N0000000121"], "upc": ["0371205992309", "0371205993306", "0371205994303"], "unii": ["9LHU78OQFD"], "rxcui": ["197903", "197904", "197905"], "spl_set_id": ["25efd38a-1495-4824-9137-a3429bc471bd"], "pharm_class_epc": ["HMG-CoA Reductase Inhibitor [EPC]"], "pharm_class_moa": ["Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71205-993-00)", "package_ndc": "71205-993-00", "marketing_start_date": "20200401"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (71205-993-11)", "package_ndc": "71205-993-11", "marketing_start_date": "20200401"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-993-30)", "package_ndc": "71205-993-30", "marketing_start_date": "20200401"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (71205-993-55)", "package_ndc": "71205-993-55", "marketing_start_date": "20200401"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-993-60)", "package_ndc": "71205-993-60", "marketing_start_date": "20200401"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-993-90)", "package_ndc": "71205-993-90", "marketing_start_date": "20200401"}], "brand_name": "Lovastatin", "product_id": "71205-993_e637904d-8af6-47fe-b10e-db813d5531bc", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "71205-993", "generic_name": "Lovastatin", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lovastatin", "active_ingredients": [{"name": "LOVASTATIN", "strength": "20 mg/1"}], "application_number": "ANDA075991", "marketing_category": "ANDA", "marketing_start_date": "20021125", "listing_expiration_date": "20261231"}