Package 71205-303-90

Brand: tramadol hydrochloride

Generic: tramadol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71205-303-90
Digits Only 7120530390
Product NDC 71205-303
Description

90 TABLET in 1 BOTTLE (71205-303-90)

Marketing

Marketing Status
Marketed Since 2019-08-01
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": "911707db-ea86-4df8-b79c-a6122d406ab0", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["835603"], "spl_set_id": ["38bd9c16-f730-4953-a444-68a95498d83c"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET in 1 BOTTLE (71205-303-15)", "package_ndc": "71205-303-15", "marketing_start_date": "20210609"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (71205-303-20)", "package_ndc": "71205-303-20", "marketing_start_date": "20190801"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-303-30)", "package_ndc": "71205-303-30", "marketing_start_date": "20190801"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE (71205-303-40)", "package_ndc": "71205-303-40", "marketing_start_date": "20190801"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-303-60)", "package_ndc": "71205-303-60", "marketing_start_date": "20190801"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71205-303-72)", "package_ndc": "71205-303-72", "marketing_start_date": "20190801"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71205-303-78)", "package_ndc": "71205-303-78", "marketing_start_date": "20190801"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-303-90)", "package_ndc": "71205-303-90", "marketing_start_date": "20190801"}], "brand_name": "tramadol hydrochloride", "product_id": "71205-303_911707db-ea86-4df8-b79c-a6122d406ab0", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "71205-303", "dea_schedule": "CIV", "generic_name": "tramadol hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "tramadol hydrochloride", "active_ingredients": [{"name": "TRAMADOL HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA075964", "marketing_category": "ANDA", "marketing_start_date": "20020622", "listing_expiration_date": "20261231"}