Package 63629-2104-1

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-2104-1
Digits Only 6362921041
Product NDC 63629-2104
Product ID 63629-2104_c3a112c7-1cfe-4a11-9b64-c4a2bcb361ce
Description

473 mL in 1 BOTTLE (63629-2104-1)

Marketing

Marketing Status
Marketed Since 2015-10-13
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": "c3a112c7-1cfe-4a11-9b64-c4a2bcb361ce", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049604"], "spl_set_id": ["e0079cc8-3642-47f0-9d14-28fd8f212c21"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (63629-2104-1)", "package_ndc": "63629-2104-1", "marketing_start_date": "20151013"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "63629-2104_c3a112c7-1cfe-4a11-9b64-c4a2bcb361ce", "dosage_form": "SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "63629-2104", "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": "5 mg/5mL"}], "application_number": "ANDA204979", "marketing_category": "ANDA", "marketing_start_date": "20151013", "listing_expiration_date": "20261231"}