Package 62559-167-01

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 62559-167-01
Digits Only 6255916701
Product NDC 62559-167
Product ID 62559-167_d6bf3c12-70dd-4089-b3ed-0d22371efbd2
Description

100 CAPSULE in 1 BOTTLE (62559-167-01)

Marketing

Marketing Status
Marketed Since 2016-06-10
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": "d6bf3c12-70dd-4089-b3ed-0d22371efbd2", "openfda": {"upc": ["0362559167017"], "unii": ["C1ENJ2TE6C"], "rxcui": ["1049696"], "spl_set_id": ["5df92fed-6194-4905-9ef2-9eed0d2e8086"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (62559-167-01)", "package_ndc": "62559-167-01", "marketing_start_date": "20160610"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "62559-167_d6bf3c12-70dd-4089-b3ed-0d22371efbd2", "dosage_form": "CAPSULE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "62559-167", "dea_schedule": "CII", "generic_name": "Oxycodone Hydrochloride", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA205177", "marketing_category": "ANDA", "marketing_start_date": "20160610", "listing_expiration_date": "20271231"}