Package 68788-8717-2
Brand: tramadol hydrochloride
Generic: tramadol hydrochloridePackage Facts
Identity
Package NDC
68788-8717-2
Digits Only
6878887172
Product NDC
68788-8717
Description
20 TABLET in 1 BOTTLE (68788-8717-2)
Marketing
Marketing Status
Brand
tramadol hydrochloride
Generic
tramadol hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "12af9122-aed2-461a-b7fc-e48a030d59a8", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["835603"], "spl_set_id": ["05f8e06b-f3eb-4cb2-aee5-bd0b03884178"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-8717-1)", "package_ndc": "68788-8717-1", "marketing_start_date": "20240718"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (68788-8717-2)", "package_ndc": "68788-8717-2", "marketing_start_date": "20240718"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8717-3)", "package_ndc": "68788-8717-3", "marketing_start_date": "20240718"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE (68788-8717-4)", "package_ndc": "68788-8717-4", "marketing_start_date": "20240718"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (68788-8717-5)", "package_ndc": "68788-8717-5", "marketing_start_date": "20240718"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-8717-6)", "package_ndc": "68788-8717-6", "marketing_start_date": "20240718"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE (68788-8717-7)", "package_ndc": "68788-8717-7", "marketing_start_date": "20240718"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (68788-8717-8)", "package_ndc": "68788-8717-8", "marketing_start_date": "20240718"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-8717-9)", "package_ndc": "68788-8717-9", "marketing_start_date": "20240718"}], "brand_name": "tramadol hydrochloride", "product_id": "68788-8717_12af9122-aed2-461a-b7fc-e48a030d59a8", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "68788-8717", "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": "50 mg/1"}], "application_number": "ANDA202075", "marketing_category": "ANDA", "marketing_start_date": "20240718", "listing_expiration_date": "20261231"}