Package 13107-057-30

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 13107-057-30
Digits Only 1310705730
Product NDC 13107-057
Product ID 13107-057_a06eea3f-6fd5-4b19-9425-4117a488c676
Description

30 TABLET in 1 BOTTLE (13107-057-30)

Marketing

Marketing Status
Marketed Since 2012-07-12
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": "a06eea3f-6fd5-4b19-9425-4117a488c676", "openfda": {"upc": ["0313107055010", "0313107056017", "0313107057014"], "unii": ["C1ENJ2TE6C"], "rxcui": ["1049611", "1049618", "1049621"], "spl_set_id": ["96ad4352-fff3-46a7-85de-466cc161045e"], "manufacturer_name": ["Aurolife Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (13107-057-01)", "package_ndc": "13107-057-01", "marketing_start_date": "20120712"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (13107-057-30)", "package_ndc": "13107-057-30", "marketing_start_date": "20120712"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (13107-057-99)", "package_ndc": "13107-057-99", "marketing_start_date": "20120712"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "13107-057_a06eea3f-6fd5-4b19-9425-4117a488c676", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "13107-057", "dea_schedule": "CII", "generic_name": "Oxycodone Hydrochloride", "labeler_name": "Aurolife Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA202160", "marketing_category": "ANDA", "marketing_start_date": "20120712", "listing_expiration_date": "20261231"}