Package 42858-302-25

{"route": ["ORAL"], "spl_id": "89fd335d-5306-4573-afca-5fdc8a25cb30", "openfda": {"upc": ["0342858303019", "0342858301015", "0342858302012"], "unii": ["L960UP2KRW"], "rxcui": ["897657", "897696", "897702", "897710"], "spl_set_id": ["37565441-0d95-4743-a695-d7b3326f58a1"], "manufacturer_name": ["Rhodes Pharmaceuticals L.P."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (42858-302-01)", "package_ndc": "42858-302-01", "marketing_start_date": "20091123"}, {"sample": false, "description": "4 BLISTER PACK in 1 CARTON (42858-302-25)  / 25 TABLET in 1 BLISTER PACK", "package_ndc": "42858-302-25", "marketing_start_date": "20091123"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (42858-302-50)", "package_ndc": "42858-302-50", "marketing_start_date": "20091123"}], "brand_name": "Hydromorphone Hydrochloride", "product_id": "42858-302_89fd335d-5306-4573-afca-5fdc8a25cb30", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "42858-302", "dea_schedule": "CII", "generic_name": "Hydromorphone Hydrochloride", "labeler_name": "Rhodes Pharmaceuticals L.P.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydromorphone Hydrochloride", "active_ingredients": [{"name": "HYDROMORPHONE HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "NDA019892", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20091123", "listing_expiration_date": "20271231"}