Package 10702-023-01

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 10702-023-01
Digits Only 1070202301
Product NDC 10702-023
Product ID 10702-023_437f25fb-bd72-c6d8-e063-6294a90a42d7
Description

100 CAPSULE in 1 BOTTLE (10702-023-01)

Marketing

Marketing Status
Marketed Since 2015-08-20
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": "437f25fb-bd72-c6d8-e063-6294a90a42d7", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049696"], "spl_set_id": ["338b5391-e5f7-40a2-8b15-57f47cbc4813"], "manufacturer_name": ["KVK-TECH, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (10702-023-01)", "package_ndc": "10702-023-01", "marketing_start_date": "20150820"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (10702-023-06)", "package_ndc": "10702-023-06", "marketing_start_date": "20150820"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "10702-023_437f25fb-bd72-c6d8-e063-6294a90a42d7", "dosage_form": "CAPSULE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "10702-023", "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": "ANDA202773", "marketing_category": "ANDA", "marketing_start_date": "20150820", "listing_expiration_date": "20261231"}