Package 10702-238-50

Brand: oxycodone and acetaminophen

Generic: oxycodone and acetaminophen
NDC Package

Package Facts

Identity

Package NDC 10702-238-50
Digits Only 1070223850
Product NDC 10702-238
Product ID 10702-238_483734fe-f7da-e43c-e063-6294a90a8191
Description

500 mL in 1 BOTTLE (10702-238-50)

Marketing

Marketing Status
Marketed Since 2019-12-05
Brand oxycodone and acetaminophen
Generic oxycodone and acetaminophen
Sample Package No

Linked Drug Pages (1)

OXYCODONE AND ACETAMINOPHEN ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "483734fe-f7da-e43c-e063-6294a90a8191", "openfda": {"unii": ["362O9ITL9D", "C1ENJ2TE6C"], "rxcui": ["1049580"], "spl_set_id": ["9986aa04-c976-4654-8ad7-b97d2eecea93"], "manufacturer_name": ["KVK-Tech, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 mL in 1 BOTTLE (10702-238-50)", "package_ndc": "10702-238-50", "marketing_start_date": "20191205"}], "brand_name": "OXYCODONE AND ACETAMINOPHEN", "product_id": "10702-238_483734fe-f7da-e43c-e063-6294a90a8191", "dosage_form": "SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "10702-238", "dea_schedule": "CII", "generic_name": "oxycodone and acetaminophen", "labeler_name": "KVK-Tech, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXYCODONE AND ACETAMINOPHEN", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/5mL"}, {"name": "OXYCODONE HYDROCHLORIDE", "strength": "5 mg/5mL"}], "application_number": "ANDA211499", "marketing_category": "ANDA", "marketing_start_date": "20191205", "listing_expiration_date": "20271231"}