Package 13107-104-99

Brand: oxymorphone hydrochloride

Generic: oxymorphone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 13107-104-99
Digits Only 1310710499
Product NDC 13107-104
Product ID 13107-104_6c5c7596-0b2c-435f-a619-706b4424370d
Description

1000 TABLET in 1 BOTTLE (13107-104-99)

Marketing

Marketing Status
Marketed Since 2016-04-26
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": "6c5c7596-0b2c-435f-a619-706b4424370d", "openfda": {"unii": ["5Y2EI94NBC"], "rxcui": ["977939", "977942"], "spl_set_id": ["22c7652a-aa16-4fa8-89d9-517e69059068"], "manufacturer_name": ["Aurolife Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (13107-104-01)", "package_ndc": "13107-104-01", "marketing_start_date": "20160426"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (13107-104-30)", "package_ndc": "13107-104-30", "marketing_start_date": "20160426"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (13107-104-99)", "package_ndc": "13107-104-99", "marketing_start_date": "20160426"}], "brand_name": "Oxymorphone Hydrochloride", "product_id": "13107-104_6c5c7596-0b2c-435f-a619-706b4424370d", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "13107-104", "dea_schedule": "CII", "generic_name": "Oxymorphone Hydrochloride", "labeler_name": "Aurolife Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxymorphone Hydrochloride", "active_ingredients": [{"name": "OXYMORPHONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA204459", "marketing_category": "ANDA", "marketing_start_date": "20160426", "listing_expiration_date": "20261231"}