Package 82868-052-30

Brand: tramadol hydrochloride

Generic: tramadol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82868-052-30
Digits Only 8286805230
Product NDC 82868-052
Product ID 82868-052_46dcc3f7-cddf-bc73-e063-6294a90a5c9c
Description

30 TABLET in 1 BOTTLE, PLASTIC (82868-052-30)

Marketing

Marketing Status
Marketed Since 2024-06-04
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": "46dcc3f7-cddf-bc73-e063-6294a90a5c9c", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["835603"], "spl_set_id": ["1b5360f8-3e95-a047-e063-6294a90a7315"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (82868-052-30)", "package_ndc": "82868-052-30", "marketing_start_date": "20240604"}], "brand_name": "tramadol hydrochloride", "product_id": "82868-052_46dcc3f7-cddf-bc73-e063-6294a90a5c9c", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "82868-052", "dea_schedule": "CIV", "generic_name": "tramadol hydrochloride", "labeler_name": "Northwind Health Company, LLC", "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": "20240604", "listing_expiration_date": "20261231"}