Package 10702-018-01

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 10702-018-01
Digits Only 1070201801
Product NDC 10702-018
Product ID 10702-018_31f901b4-04ad-38aa-e063-6294a90ac708
Description

100 TABLET in 1 BOTTLE (10702-018-01)

Marketing

Marketing Status
Marketed Since 2013-10-18
Brand oxycodone hydrochloride
Generic oxycodone hydrochloride
Sample Package No

Linked Drug Pages (1)

OXYCODONE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "31f901b4-04ad-38aa-e063-6294a90ac708", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049611", "1049618", "1049621", "1049683", "1049686"], "spl_set_id": ["e73897d6-b920-4300-a564-5dbc9c8e9fe9"], "manufacturer_name": ["KVK-TECH,INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (10702-018-01)", "package_ndc": "10702-018-01", "marketing_start_date": "20131018"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (10702-018-50)", "package_ndc": "10702-018-50", "marketing_start_date": "20131018"}], "brand_name": "OXYCODONE HYDROCHLORIDE", "product_id": "10702-018_31f901b4-04ad-38aa-e063-6294a90ac708", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "10702-018", "dea_schedule": "CII", "generic_name": "OXYCODONE HYDROCHLORIDE", "labeler_name": "KVK-TECH,INC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXYCODONE HYDROCHLORIDE", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA091393", "marketing_category": "ANDA", "marketing_start_date": "20131018", "listing_expiration_date": "20261231"}