Package 68788-7601-3

{"route": ["ORAL"], "spl_id": "002cc3ab-993f-4e80-a885-c07bfd4b5dc1", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["833711"], "spl_set_id": ["83367367-5654-4078-831a-69ade48bc795"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7601-2)", "package_ndc": "68788-7601-2", "marketing_start_date": "20200206"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7601-3)", "package_ndc": "68788-7601-3", "marketing_start_date": "20200206"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7601-6)", "package_ndc": "68788-7601-6", "marketing_start_date": "20200206"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7601-9)", "package_ndc": "68788-7601-9", "marketing_start_date": "20200206"}], "brand_name": "TRAMADOL HYDROCHLORIDE", "product_id": "68788-7601_002cc3ab-993f-4e80-a885-c07bfd4b5dc1", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "68788-7601", "dea_schedule": "CIV", "generic_name": "TRAMADOL HYDROCHLORIDE", "labeler_name": "Preferred Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TRAMADOL HYDROCHLORIDE", "active_ingredients": [{"name": "TRAMADOL HYDROCHLORIDE", "strength": "200 mg/1"}], "application_number": "ANDA200503", "marketing_category": "ANDA", "marketing_start_date": "20200206", "listing_expiration_date": "20261231"}