Package 70518-0297-0

{"route": ["ORAL"], "spl_id": "47e699d6-cdb8-0be8-e063-6294a90a8870", "openfda": {"unii": ["864V2Q084H"], "rxcui": ["308135"], "spl_set_id": ["a6fa364c-3ad6-4bf9-b9ee-5ec3b1a7eb55"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-0297-0)", "package_ndc": "70518-0297-0", "marketing_start_date": "20170308"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-0297-1)", "package_ndc": "70518-0297-1", "marketing_start_date": "20170424"}], "brand_name": "AMLODIPINE BESYLATE", "product_id": "70518-0297_47e699d6-cdb8-0be8-e063-6294a90a8870", "dosage_form": "TABLET", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A Inhibitors [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "70518-0297", "generic_name": "AMLODIPINE BESYLATE", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AMLODIPINE BESYLATE", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "10 mg/1"}], "application_number": "ANDA077073", "marketing_category": "ANDA", "marketing_start_date": "20170308", "listing_expiration_date": "20271231"}