Package 51662-1545-1

Brand: rocuronium bromide

Generic: rocuronium bromide
NDC Package

Package Facts

Identity

Package NDC 51662-1545-1
Digits Only 5166215451
Product NDC 51662-1545
Description

10 mL in 1 VIAL, MULTI-DOSE (51662-1545-1)

Marketing

Marketing Status
Marketed Since 2022-04-09
Brand rocuronium bromide
Generic rocuronium bromide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "dc444a4b-16eb-568d-e053-2995a90a53a7", "openfda": {"unii": ["I65MW4OFHZ"], "rxcui": ["1234995"], "spl_set_id": ["dc444a4b-16ea-568d-e053-2995a90a53a7"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "10 mL in 1 VIAL, MULTI-DOSE (51662-1545-1)", "package_ndc": "51662-1545-1", "marketing_start_date": "20220409"}], "brand_name": "ROCURONIUM BROMIDE", "product_id": "51662-1545_dc444a4b-16eb-568d-e053-2995a90a53a7", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Neuromuscular Nondepolarizing Blockade [PE]", "Nondepolarizing Neuromuscular Blocker [EPC]"], "product_ndc": "51662-1545", "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": "100 mg/10mL"}], "application_number": "ANDA206206", "marketing_category": "ANDA", "marketing_start_date": "20220409", "listing_expiration_date": "20261231"}