Package 63323-853-25

Brand: hydromorphone hydrochloride

Generic: hydromorphone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63323-853-25
Digits Only 6332385325
Product NDC 63323-853
Product ID 63323-853_9e8522c6-595c-46f9-bb25-272aa4683e0f
Description

25 VIAL, SINGLE-DOSE in 1 CARTON (63323-853-25) / 1 mL in 1 VIAL, SINGLE-DOSE (63323-853-03)

Marketing

Marketing Status
Marketed Since 2017-12-15
Brand hydromorphone hydrochloride
Generic hydromorphone hydrochloride
Sample Package No

Linked Drug Pages (1)

Hydromorphone Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "9e8522c6-595c-46f9-bb25-272aa4683e0f", "openfda": {"upc": ["0363323851507", "0363323853037", "0363323852030", "0363323851071", "0363323854034", "0363323851033"], "unii": ["L960UP2KRW"], "rxcui": ["897653", "897753", "1724276", "1724338", "1724340", "1724341"], "spl_set_id": ["e034eb96-03e0-46e1-8b92-5e1f94555e7b"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (63323-853-25)  / 1 mL in 1 VIAL, SINGLE-DOSE (63323-853-03)", "package_ndc": "63323-853-25", "marketing_start_date": "20171215"}], "brand_name": "Hydromorphone Hydrochloride", "product_id": "63323-853_9e8522c6-595c-46f9-bb25-272aa4683e0f", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "63323-853", "dea_schedule": "CII", "generic_name": "Hydromorphone Hydrochloride", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydromorphone Hydrochloride", "active_ingredients": [{"name": "HYDROMORPHONE HYDROCHLORIDE", "strength": "2 mg/mL"}], "application_number": "NDA019034", "marketing_category": "NDA", "marketing_start_date": "20171215", "listing_expiration_date": "20261231"}