Package 72189-311-20
Brand: tramadol hydrochloride
Generic: tramadol hydrochloridePackage Facts
Identity
Package NDC
72189-311-20
Digits Only
7218931120
Product NDC
72189-311
Description
20 TABLET, COATED in 1 BOTTLE (72189-311-20)
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": "2c3cf1d7-38f5-4d25-e063-6294a90aa8cd", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["835603"], "spl_set_id": ["d5685c80-c84d-d0a1-e053-2995a90afc54"], "manufacturer_name": ["DirectRx"]}, "finished": true, "packaging": [{"sample": false, "description": "12 TABLET, COATED in 1 BOTTLE (72189-311-12)", "package_ndc": "72189-311-12", "marketing_start_date": "20220112"}, {"sample": false, "description": "20 TABLET, COATED in 1 BOTTLE (72189-311-20)", "package_ndc": "72189-311-20", "marketing_start_date": "20220112"}, {"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (72189-311-30)", "package_ndc": "72189-311-30", "marketing_start_date": "20220112"}, {"sample": false, "description": "40 TABLET, COATED in 1 BOTTLE (72189-311-40)", "package_ndc": "72189-311-40", "marketing_start_date": "20220112"}, {"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE (72189-311-60)", "package_ndc": "72189-311-60", "marketing_start_date": "20220112"}, {"sample": false, "description": "120 TABLET, COATED in 1 BOTTLE (72189-311-72)", "package_ndc": "72189-311-72", "marketing_start_date": "20220112"}, {"sample": false, "description": "180 TABLET, COATED in 1 BOTTLE (72189-311-82)", "package_ndc": "72189-311-82", "marketing_start_date": "20220112"}, {"sample": false, "description": "240 TABLET, COATED in 1 BOTTLE (72189-311-84)", "package_ndc": "72189-311-84", "marketing_start_date": "20220112"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (72189-311-90)", "package_ndc": "72189-311-90", "marketing_start_date": "20220112"}], "brand_name": "TRAMADOL HYDROCHLORIDE", "product_id": "72189-311_2c3cf1d7-38f5-4d25-e063-6294a90aa8cd", "dosage_form": "TABLET, COATED", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72189-311", "dea_schedule": "CIV", "generic_name": "TRAMADOL HYDROCHLORIDE", "labeler_name": "DirectRx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TRAMADOL HYDROCHLORIDE", "active_ingredients": [{"name": "TRAMADOL HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA208708", "marketing_category": "ANDA", "marketing_start_date": "20220112", "listing_expiration_date": "20261231"}