Package 45865-184-30

Brand: tramadol hydrochloride

Generic: tramadol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 45865-184-30
Digits Only 4586518430
Product NDC 45865-184
Product ID 45865-184_12789848-2a06-0414-e063-6394a90a3d50
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (45865-184-30)

Marketing

Marketing Status
Marketed Since 2021-05-28
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": "12789848-2a06-0414-e063-6394a90a3d50", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["833713"], "spl_set_id": ["1278980b-4068-df57-e063-6394a90a8742"], "manufacturer_name": ["Medsource Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (45865-184-30)", "package_ndc": "45865-184-30", "marketing_start_date": "20210528"}], "brand_name": "TRAMADOL HYDROCHLORIDE", "product_id": "45865-184_12789848-2a06-0414-e063-6394a90a3d50", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "45865-184", "dea_schedule": "CIV", "generic_name": "TRAMADOL HYDROCHLORIDE", "labeler_name": "Medsource Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TRAMADOL HYDROCHLORIDE", "active_ingredients": [{"name": "TRAMADOL HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA200503", "marketing_category": "ANDA", "marketing_start_date": "20140819", "listing_expiration_date": "20261231"}