Package 76045-121-11

Brand: dilaudid

Generic: hydromorphone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 76045-121-11
Digits Only 7604512111
Product NDC 76045-121
Product ID 76045-121_97bfcafb-2037-47dc-a0ae-f7b8007c47df
Description

10 SYRINGE in 1 CARTON (76045-121-11) / 1 mL in 1 SYRINGE (76045-121-01)

Marketing

Marketing Status
Marketed Since 2020-01-16
Brand dilaudid
Generic hydromorphone hydrochloride
Sample Package No

Linked Drug Pages (1)

Dilaudid ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "97bfcafb-2037-47dc-a0ae-f7b8007c47df", "openfda": {"unii": ["L960UP2KRW"], "rxcui": ["897756", "897757", "1433251", "1872265", "1872269", "1872752", "2277368", "2277370"], "spl_set_id": ["9eebd88a-5632-460f-b7b6-26c8a180540d"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 SYRINGE in 1 CARTON (76045-121-11)  / 1 mL in 1 SYRINGE (76045-121-01)", "package_ndc": "76045-121-11", "marketing_start_date": "20200116"}], "brand_name": "Dilaudid", "product_id": "76045-121_97bfcafb-2037-47dc-a0ae-f7b8007c47df", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "76045-121", "dea_schedule": "CII", "generic_name": "Hydromorphone hydrochloride", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dilaudid", "active_ingredients": [{"name": "HYDROMORPHONE HYDROCHLORIDE", "strength": ".2 mg/mL"}], "application_number": "NDA019034", "marketing_category": "NDA", "marketing_start_date": "20161216", "listing_expiration_date": "20261231"}