Package 60505-3493-3

{"route": ["ORAL"], "spl_id": "f3120a95-7f28-006c-6bf7-12c962071ed9", "openfda": {"upc": ["0360505347933", "0360505349333", "0360505348930", "0360505348435", "0360505348336", "0360505347834"], "unii": ["48A5M73Z4Q", "864V2Q084H"], "rxcui": ["404011", "404013", "597967", "597977", "597980", "597984", "597987", "597990"], "spl_set_id": ["4c7b1b11-90a3-bc1c-0e45-9e2a14ef0b03"], "manufacturer_name": ["Apotex Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (60505-3493-3)", "package_ndc": "60505-3493-3", "marketing_start_date": "20200729"}], "brand_name": "Amlodipine and Atorvastatin", "product_id": "60505-3493_f3120a95-7f28-006c-6bf7-12c962071ed9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A Inhibitors [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]", "HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "60505-3493", "generic_name": "Amlodipine and Atorvastatin", "labeler_name": "Apotex Corp.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amlodipine and Atorvastatin", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "10 mg/1"}, {"name": "ATORVASTATIN CALCIUM TRIHYDRATE", "strength": "80 mg/1"}], "application_number": "ANDA205199", "marketing_category": "ANDA", "marketing_start_date": "20200729", "listing_expiration_date": "20261231"}