Package 0115-1234-03
Brand: oxymorphone hydrochloride
Generic: oxymorphone hydrochloridePackage Facts
Identity
Package NDC
0115-1234-03
Digits Only
0115123403
Product NDC
0115-1234
Description
1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1234-03)
Marketing
Marketing Status
Brand
oxymorphone hydrochloride
Generic
oxymorphone hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a8dc6624-df1e-4e5a-b445-9541658e3430", "openfda": {"unii": ["5Y2EI94NBC"], "rxcui": ["977874", "977894", "977902", "977909", "977915", "977923", "977929"], "spl_set_id": ["557e9610-62d7-42bf-90c1-44215bd8c1f8"], "manufacturer_name": ["Amneal Pharmaceuticals of New York LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1234-01)", "package_ndc": "0115-1234-01", "marketing_start_date": "20130102"}, {"sample": false, "description": "1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1234-03)", "package_ndc": "0115-1234-03", "marketing_start_date": "20130102"}, {"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1234-08)", "package_ndc": "0115-1234-08", "marketing_start_date": "20130102"}, {"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1234-13)", "package_ndc": "0115-1234-13", "marketing_start_date": "20130102"}], "brand_name": "Oxymorphone hydrochloride", "product_id": "0115-1234_a8dc6624-df1e-4e5a-b445-9541658e3430", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0115-1234", "dea_schedule": "CII", "generic_name": "Oxymorphone hydrochloride", "labeler_name": "Amneal Pharmaceuticals of New York LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxymorphone hydrochloride", "active_ingredients": [{"name": "OXYMORPHONE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA079087", "marketing_category": "ANDA", "marketing_start_date": "20130102", "listing_expiration_date": "20261231"}