Package 0406-8557-30

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0406-8557-30
Digits Only 0406855730
Product NDC 0406-8557
Description

1 BOTTLE, PLASTIC in 1 CARTON (0406-8557-30) / 30 mL in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2018-04-30
Brand oxycodone hydrochloride
Generic oxycodone hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7e788fe5-6049-4ff6-a09a-60e8b9e52d9d", "openfda": {"upc": ["0304068556050", "0304068557309"], "unii": ["C1ENJ2TE6C"], "rxcui": ["1049604", "1049615"], "spl_set_id": ["5451bcaa-0aca-4581-bcea-2f9c2a33b260"], "manufacturer_name": ["SpecGx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (0406-8557-30)  / 30 mL in 1 BOTTLE, PLASTIC", "package_ndc": "0406-8557-30", "marketing_start_date": "20180430"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "0406-8557_7e788fe5-6049-4ff6-a09a-60e8b9e52d9d", "dosage_form": "SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0406-8557", "dea_schedule": "CII", "generic_name": "Oxycodone Hydrochloride", "labeler_name": "SpecGx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "100 mg/5mL"}], "application_number": "ANDA210758", "marketing_category": "ANDA", "marketing_start_date": "20180430", "listing_expiration_date": "20261231"}