Package 43602-190-50

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43602-190-50
Digits Only 4360219050
Product NDC 43602-190
Description

500 mL in 1 BOTTLE (43602-190-50)

Marketing

Marketing Status
Marketed Since 2017-07-13
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": "46183e47-ba04-4b02-912a-6aeed41c609e", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049604", "1049615"], "spl_set_id": ["de96e2be-66d9-4bcb-a133-221ad32e09f1"], "manufacturer_name": ["Ascent Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 BOTTLE (43602-190-31)", "package_ndc": "43602-190-31", "marketing_start_date": "20170713"}, {"sample": false, "description": "500 mL in 1 BOTTLE (43602-190-50)", "package_ndc": "43602-190-50", "marketing_start_date": "20170713"}], "brand_name": "OXYCODONE HYDROCHLORIDE", "product_id": "43602-190_46183e47-ba04-4b02-912a-6aeed41c609e", "dosage_form": "SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "43602-190", "dea_schedule": "CII", "generic_name": "OXYCODONE HYDROCHLORIDE", "labeler_name": "Ascent Pharmaceuticals Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXYCODONE HYDROCHLORIDE", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "5 mg/5mL"}], "application_number": "ANDA209021", "marketing_category": "ANDA", "marketing_start_date": "20170713", "listing_expiration_date": "20261231"}