Package 82647-210-30

{"route": ["ORAL"], "spl_id": "49fd0cc5-980e-c7d1-e063-6394a90a85c0", "openfda": {"upc": ["0382647211149", "0382647210142"], "unii": ["BW9B0ZE037"], "rxcui": ["312950", "314228", "314229"], "spl_set_id": ["dc998a9c-0770-111b-e053-2a95a90a88a4"], "manufacturer_name": ["Reyoung Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (82647-210-14)", "package_ndc": "82647-210-14", "marketing_start_date": "20220328"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (82647-210-30)", "package_ndc": "82647-210-30", "marketing_start_date": "20220328"}], "brand_name": "Sildenafil", "product_id": "82647-210_49fd0cc5-980e-c7d1-e063-6394a90a85c0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "82647-210", "generic_name": "sildenafil", "labeler_name": "Reyoung Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "25 mg/1"}], "application_number": "ANDA208494", "marketing_category": "ANDA", "marketing_start_date": "20220328", "listing_expiration_date": "20271231"}