Package 76420-061-90

{"route": ["ORAL"], "spl_id": "e785ec65-b5e8-693c-e053-2995a90aa9e7", "openfda": {"unii": ["BW9B0ZE037"], "rxcui": ["577033"], "spl_set_id": ["06571775-b651-4e23-a35b-88392aae7e13"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (76420-061-30)", "package_ndc": "76420-061-30", "marketing_start_date": "20191210"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (76420-061-60)", "package_ndc": "76420-061-60", "marketing_start_date": "20220831"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (76420-061-90)", "package_ndc": "76420-061-90", "marketing_start_date": "20191210"}], "brand_name": "Sildenafil", "product_id": "76420-061_e785ec65-b5e8-693c-e053-2995a90aa9e7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "76420-061", "generic_name": "Sildenafil", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "20 mg/1"}], "application_number": "ANDA203814", "marketing_category": "ANDA", "marketing_start_date": "20140103", "listing_expiration_date": "20261231"}