Package 83008-009-30

Brand: tramadol hydrochloride

Generic: tramadol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 83008-009-30
Digits Only 8300800930
Product NDC 83008-009
Product ID 83008-009_6e6ef0b4-62eb-4258-af63-6ba7cbd023b6
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (83008-009-30)

Marketing

Marketing Status
Discontinued 2027-01-31
Brand tramadol hydrochloride
Generic tramadol hydrochloride
Sample Package No

Linked Drug Pages (1)

TRAMADOL HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "6e6ef0b4-62eb-4258-af63-6ba7cbd023b6", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["833711"], "spl_set_id": ["68484531-f908-473f-a422-f37234de9691"], "manufacturer_name": ["Quality Care Products, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (83008-009-30)", "package_ndc": "83008-009-30", "marketing_end_date": "20270131", "marketing_start_date": "20230303"}], "brand_name": "TRAMADOL HYDROCHLORIDE", "product_id": "83008-009_6e6ef0b4-62eb-4258-af63-6ba7cbd023b6", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "83008-009", "dea_schedule": "CIV", "generic_name": "TRAMADOL HYDROCHLORIDE", "labeler_name": "Quality Care Products, LLC", "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_end_date": "20270131", "marketing_start_date": "20230303"}