Package 63323-426-15

Brand: rocuronium

Generic: rocuronium bromide
NDC Package

Package Facts

Identity

Package NDC 63323-426-15
Digits Only 6332342615
Product NDC 63323-426
Description

10 VIAL in 1 TRAY (63323-426-15) / 5 mL in 1 VIAL (63323-426-12)

Marketing

Marketing Status
Marketed Since 2009-12-13
Brand rocuronium
Generic rocuronium bromide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "3f4d5e11-2c14-4406-8954-04dba2fc65ff", "openfda": {"upc": ["0363323426125"], "unii": ["I65MW4OFHZ"], "rxcui": ["1234995"], "spl_set_id": ["fb9524b2-c353-4747-8954-7ca2529eabb2"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 TRAY (63323-426-15)  / 5 mL in 1 VIAL (63323-426-12)", "package_ndc": "63323-426-15", "marketing_start_date": "20091213"}], "brand_name": "Rocuronium", "product_id": "63323-426_3f4d5e11-2c14-4406-8954-04dba2fc65ff", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Neuromuscular Nondepolarizing Blockade [PE]", "Nondepolarizing Neuromuscular Blocker [EPC]"], "product_ndc": "63323-426", "generic_name": "ROCURONIUM BROMIDE", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Rocuronium", "active_ingredients": [{"name": "ROCURONIUM BROMIDE", "strength": "10 mg/mL"}], "application_number": "ANDA078651", "marketing_category": "ANDA", "marketing_start_date": "20091213", "listing_expiration_date": "20261231"}