Package 60760-957-60

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-957-60
Digits Only 6076095760
Product NDC 60760-957
Product ID 60760-957_424fdde3-5cd5-2771-e063-6294a90aa37f
Description

60 TABLET in 1 BOTTLE, PLASTIC (60760-957-60)

Marketing

Marketing Status
Marketed Since 2025-10-29
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": "424fdde3-5cd5-2771-e063-6294a90aa37f", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049611"], "spl_set_id": ["424fdfc7-1c92-2e62-e063-6394a90a136b"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (60760-957-60)", "package_ndc": "60760-957-60", "marketing_start_date": "20251029"}], "brand_name": "OXYCODONE HYDROCHLORIDE", "product_id": "60760-957_424fdde3-5cd5-2771-e063-6294a90aa37f", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "60760-957", "dea_schedule": "CII", "generic_name": "OXYCODONE HYDROCHLORIDE", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXYCODONE HYDROCHLORIDE", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA091393", "marketing_category": "ANDA", "marketing_start_date": "20131018", "listing_expiration_date": "20261231"}