Package 65862-617-55

{"route": ["ORAL"], "spl_id": "5263abd5-ce46-4918-9bb0-9632861bcbc9", "openfda": {"upc": ["0365862618900", "0365862617903", "0365862619907"], "unii": ["33067B3N2M"], "rxcui": ["312748", "312749", "312750", "314203"], "spl_set_id": ["93e6e668-5306-4f26-81d8-cbc3a7a5e787"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (65862-617-30)", "package_ndc": "65862-617-30", "marketing_start_date": "20130429"}, {"sample": false, "description": "15000 TABLET, FILM COATED in 1 BOTTLE (65862-617-55)", "package_ndc": "65862-617-55", "marketing_start_date": "20130429"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (65862-617-78)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-617-10)", "package_ndc": "65862-617-78", "marketing_start_date": "20130429"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (65862-617-90)", "package_ndc": "65862-617-90", "marketing_start_date": "20130429"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (65862-617-99)", "package_ndc": "65862-617-99", "marketing_start_date": "20130429"}], "brand_name": "Quinapril", "product_id": "65862-617_5263abd5-ce46-4918-9bb0-9632861bcbc9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "65862-617", "generic_name": "Quinapril Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quinapril", "active_ingredients": [{"name": "QUINAPRIL HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA202725", "marketing_category": "ANDA", "marketing_start_date": "20130429", "listing_expiration_date": "20261231"}