Package 72189-154-60
Brand: tramadol hydrochloride
Generic: tramadol hydrochloridePackage Facts
Identity
Package NDC
72189-154-60
Digits Only
7218915460
Product NDC
72189-154
Description
60 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-154-60)
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": "2be91ca4-b100-8b02-e063-6294a90a3c24", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["833711"], "spl_set_id": ["b3c702f7-0a8c-a52b-e053-2995a90a6df3"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-154-30)", "package_ndc": "72189-154-30", "marketing_start_date": "20201110"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-154-60)", "package_ndc": "72189-154-60", "marketing_start_date": "20201110"}], "brand_name": "TRAMADOL HYDROCHLORIDE", "product_id": "72189-154_2be91ca4-b100-8b02-e063-6294a90a3c24", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72189-154", "dea_schedule": "CIV", "generic_name": "TRAMADOL HYDROCHLORIDE", "labeler_name": "DIRECT RX", "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": "20201110", "listing_expiration_date": "20261231"}