Package 10702-183-50

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 10702-183-50
Digits Only 1070218350
Product NDC 10702-183
Product ID 10702-183_441eb113-64da-ceeb-e063-6394a90a2f74
Description

1 BOTTLE, PLASTIC in 1 CARTON (10702-183-50) / 500 mL in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2017-07-21
Brand oxycodone hydrochloride
Generic oxycodone hydrochloride
Sample Package No

Linked Drug Pages (1)

OXYCODONE HYDROCHLORIDE, Oxycodone Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "441eb113-64da-ceeb-e063-6394a90a2f74", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049604", "1049615"], "spl_set_id": ["744f5d1c-7427-492c-8994-c8e817793e53"], "manufacturer_name": ["KVK-Tech, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (10702-183-50)  / 500 mL in 1 BOTTLE, PLASTIC", "package_ndc": "10702-183-50", "marketing_start_date": "20170721"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "10702-183_441eb113-64da-ceeb-e063-6394a90a2f74", "dosage_form": "SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "10702-183", "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/5mL"}], "application_number": "ANDA208593", "marketing_category": "ANDA", "marketing_start_date": "20170721", "listing_expiration_date": "20261231"}