Package 42858-203-90

{"route": ["ORAL"], "spl_id": "121d5573-efb2-4cc3-8a1e-9dd7adfee4d3", "openfda": {"upc": ["0342858202015", "0342858201018", "0342858203012"], "unii": ["NO70W886KK", "362O9ITL9D"], "rxcui": ["856999", "857002", "857005"], "spl_set_id": ["1f9c1adc-f84f-43de-af5c-d93703aba7f8"], "manufacturer_name": ["Rhodes Pharmaceuticals L.P."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (42858-203-01)", "package_ndc": "42858-203-01", "marketing_start_date": "20160412"}, {"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (42858-203-10)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "42858-203-10", "marketing_start_date": "20160412"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (42858-203-50)", "package_ndc": "42858-203-50", "marketing_start_date": "20160412"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (42858-203-90)", "package_ndc": "42858-203-90", "marketing_start_date": "20160412"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "42858-203_121d5573-efb2-4cc3-8a1e-9dd7adfee4d3", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "42858-203", "dea_schedule": "CII", "generic_name": "Hydrocodone Bitartrate and Acetaminophen", "labeler_name": "Rhodes Pharmaceuticals L.P.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrocodone Bitartrate and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "HYDROCODONE BITARTRATE", "strength": "10 mg/1"}], "application_number": "ANDA202991", "marketing_category": "ANDA", "marketing_start_date": "20160412", "listing_expiration_date": "20271231"}