Package 51662-1355-1

Brand: rocuronium bromide

Generic: rocuronium bromide
NDC Package

Package Facts

Identity

Package NDC 51662-1355-1
Digits Only 5166213551
Product NDC 51662-1355
Product ID 51662-1355_bc7f145c-81b3-f8e7-e053-2a95a90add55
Description

10 mL in 1 VIAL, MULTI-DOSE (51662-1355-1)

Marketing

Marketing Status
Marketed Since 2019-02-10
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": "bc7f145c-81b3-f8e7-e053-2a95a90add55", "openfda": {"unii": ["I65MW4OFHZ"], "rxcui": ["1234995"], "spl_set_id": ["818f7cc6-2c3f-1788-e053-2991aa0a4c6a"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "10 mL in 1 VIAL, MULTI-DOSE (51662-1355-1)", "package_ndc": "51662-1355-1", "marketing_start_date": "20190210"}], "brand_name": "ROCURONIUM BROMIDE", "product_id": "51662-1355_bc7f145c-81b3-f8e7-e053-2a95a90add55", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Neuromuscular Nondepolarizing Blockade [PE]", "Nondepolarizing Neuromuscular Blocker [EPC]"], "product_ndc": "51662-1355", "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": "20190210", "listing_expiration_date": "20261231"}