Package 62559-151-16

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 62559-151-16
Digits Only 6255915116
Product NDC 62559-151
Product ID 62559-151_2dd00699-5e0a-42cd-8b52-0d8025d37d39
Description

1 BOTTLE in 1 CARTON (62559-151-16) / 473 mL in 1 BOTTLE

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": "2dd00699-5e0a-42cd-8b52-0d8025d37d39", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049604"], "spl_set_id": ["819ed9fc-0a21-4ed0-9080-91912c5f8ce2"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (62559-151-16)  / 473 mL in 1 BOTTLE", "package_ndc": "62559-151-16", "marketing_start_date": "20151013"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "62559-151_2dd00699-5e0a-42cd-8b52-0d8025d37d39", "dosage_form": "SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "62559-151", "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/5mL"}], "application_number": "ANDA204979", "marketing_category": "ANDA", "marketing_start_date": "20151013", "listing_expiration_date": "20271231"}