Package 63629-1930-1

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-1930-1
Digits Only 6362919301
Product NDC 63629-1930
Product ID 63629-1930_06c695ae-e538-4c96-8f41-f988c38b1c0a
Description

500 TABLET in 1 BOTTLE (63629-1930-1)

Marketing

Marketing Status
Marketed Since 2017-08-08
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": "06c695ae-e538-4c96-8f41-f988c38b1c0a", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049618"], "spl_set_id": ["35030c55-47e6-44cb-9d96-0c3cd5d0c238"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (63629-1930-1)", "package_ndc": "63629-1930-1", "marketing_start_date": "20170808"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "63629-1930_06c695ae-e538-4c96-8f41-f988c38b1c0a", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "63629-1930", "dea_schedule": "CII", "generic_name": "Oxycodone Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA207418", "marketing_category": "ANDA", "marketing_start_date": "20170808", "listing_expiration_date": "20261231"}