Package 63629-1174-1

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-1174-1
Digits Only 6362911741
Product NDC 63629-1174
Product ID 63629-1174_e3771799-f37b-4b63-bc47-169c76cf7488
Description

1 BOTTLE in 1 CARTON (63629-1174-1) / 473 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2019-03-01
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": "e3771799-f37b-4b63-bc47-169c76cf7488", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049604"], "spl_set_id": ["e2e52a0e-a80b-4225-b034-37a62f839d92"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (63629-1174-1)  / 473 mL in 1 BOTTLE", "package_ndc": "63629-1174-1", "marketing_start_date": "20190301"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "63629-1174_e3771799-f37b-4b63-bc47-169c76cf7488", "dosage_form": "SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "63629-1174", "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": "ANDA207511", "marketing_category": "ANDA", "marketing_start_date": "20190301", "listing_expiration_date": "20261231"}