Package 51662-1354-1

Brand: rocuronium bromide

Generic: rocuronium bromide
NDC Package

Package Facts

Identity

Package NDC 51662-1354-1
Digits Only 5166213541
Product NDC 51662-1354
Product ID 51662-1354_100db255-132c-7c4f-e063-6294a90a01fc
Description

5 mL in 1 VIAL, MULTI-DOSE (51662-1354-1)

Marketing

Marketing Status
Marketed Since 2019-02-08
Brand rocuronium bromide
Generic rocuronium bromide
Sample Package No

Linked Drug Pages (1)

ROCURONIUM BROMIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "100db255-132c-7c4f-e063-6294a90a01fc", "openfda": {"unii": ["I65MW4OFHZ"], "rxcui": ["1234995"], "spl_set_id": ["81628de9-e6bf-8f69-e053-2991aa0a6023"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "5 mL in 1 VIAL, MULTI-DOSE (51662-1354-1)", "package_ndc": "51662-1354-1", "marketing_start_date": "20190208"}], "brand_name": "ROCURONIUM BROMIDE", "product_id": "51662-1354_100db255-132c-7c4f-e063-6294a90a01fc", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Neuromuscular Nondepolarizing Blockade [PE]", "Nondepolarizing Neuromuscular Blocker [EPC]"], "product_ndc": "51662-1354", "generic_name": "ROCURONIUM BROMIDE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ROCURONIUM BROMIDE", "active_ingredients": [{"name": "ROCURONIUM BROMIDE", "strength": "10 mg/mL"}], "application_number": "ANDA078519", "marketing_category": "ANDA", "marketing_start_date": "20190208", "listing_expiration_date": "20261231"}