Package 71930-023-30

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71930-023-30
Digits Only 7193002330
Product NDC 71930-023
Product ID 71930-023_353e35c4-e3fa-46d0-8497-8872b8c53c39
Description

1 BOTTLE in 1 CARTON (71930-023-30) / 30 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2018-06-01
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": "353e35c4-e3fa-46d0-8497-8872b8c53c39", "openfda": {"upc": ["0371930023309"], "unii": ["C1ENJ2TE6C"], "rxcui": ["1049615"], "spl_set_id": ["c801963d-f54d-4ed5-82c4-8b278528d3dc"], "manufacturer_name": ["Eywa Pharma Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (71930-023-30)  / 30 mL in 1 BOTTLE", "package_ndc": "71930-023-30", "marketing_start_date": "20180601"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "71930-023_353e35c4-e3fa-46d0-8497-8872b8c53c39", "dosage_form": "SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "71930-023", "dea_schedule": "CII", "generic_name": "Oxycodone hydrochloride", "labeler_name": "Eywa Pharma Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA209897", "marketing_category": "ANDA", "marketing_start_date": "20180601", "listing_expiration_date": "20271231"}