Package 0781-6156-57

{"route": ["ORAL"], "spl_id": "6aa02079-d11c-4d2f-acaf-9548dd9a7ed6", "openfda": {"upc": ["0307816156526", "0307812020012", "0307816041587", "0307815060015", "0307815061012", "0307816157523", "0307816039584", "0307812613016"], "unii": ["804826J2HU"], "rxcui": ["239191", "308182", "308189", "308191", "308192", "308194", "313797", "313850"], "spl_set_id": ["13bd4214-9b7f-425b-af5f-fc1ddc678230"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (0781-6156-46)", "package_ndc": "0781-6156-46", "marketing_start_date": "20070326"}, {"sample": false, "description": "50 mL in 1 BOTTLE (0781-6156-52)", "package_ndc": "0781-6156-52", "marketing_start_date": "20070326"}, {"sample": false, "description": "75 mL in 1 BOTTLE (0781-6156-57)", "package_ndc": "0781-6156-57", "marketing_start_date": "20070326"}], "brand_name": "Amoxicillin", "product_id": "0781-6156_6aa02079-d11c-4d2f-acaf-9548dd9a7ed6", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "0781-6156", "generic_name": "Amoxicillin", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "200 mg/5mL"}], "application_number": "ANDA065378", "marketing_category": "ANDA", "marketing_start_date": "20070326", "listing_expiration_date": "20261231"}