Package 10702-070-01

Brand: oxymorphone hydrochloride

Generic: oxymorphone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 10702-070-01
Digits Only 1070207001
Product NDC 10702-070
Product ID 10702-070_499ffc26-7516-aea3-e063-6394a90a5845
Description

100 TABLET in 1 BOTTLE (10702-070-01)

Marketing

Marketing Status
Marketed Since 2013-02-11
Brand oxymorphone hydrochloride
Generic oxymorphone hydrochloride
Sample Package No

Linked Drug Pages (1)

Oxymorphone Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "499ffc26-7516-aea3-e063-6394a90a5845", "openfda": {"unii": ["5Y2EI94NBC"], "rxcui": ["977939", "977942"], "spl_set_id": ["dcb5b5d2-7d0a-497a-8f1e-3b96fd43320b"], "manufacturer_name": ["KVK-Tech, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (10702-070-01)", "package_ndc": "10702-070-01", "marketing_start_date": "20130211"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (10702-070-06)", "package_ndc": "10702-070-06", "marketing_start_date": "20180625"}], "brand_name": "Oxymorphone Hydrochloride", "product_id": "10702-070_499ffc26-7516-aea3-e063-6394a90a5845", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "10702-070", "dea_schedule": "CII", "generic_name": "Oxymorphone Hydrochloride", "labeler_name": "KVK-Tech, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxymorphone Hydrochloride", "active_ingredients": [{"name": "OXYMORPHONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA203601", "marketing_category": "ANDA", "marketing_start_date": "20130211", "listing_expiration_date": "20271231"}