Package 71930-022-43

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71930-022-43
Digits Only 7193002243
Product NDC 71930-022
Product ID 71930-022_d5dbbf3c-6269-488c-b3a2-9539f45e3945
Description

1 BOTTLE in 1 CARTON (71930-022-43) / 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": "d5dbbf3c-6269-488c-b3a2-9539f45e3945", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049604"], "spl_set_id": ["685f409f-946f-4b7e-8130-5ad7b92a5e7a"], "manufacturer_name": ["Eywa Pharma Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (71930-022-43)  / 473 mL in 1 BOTTLE", "package_ndc": "71930-022-43", "marketing_start_date": "20190301"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "71930-022_d5dbbf3c-6269-488c-b3a2-9539f45e3945", "dosage_form": "SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "71930-022", "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": "5 mg/5mL"}], "application_number": "ANDA207511", "marketing_category": "ANDA", "marketing_start_date": "20190301", "listing_expiration_date": "20271231"}