Package 51662-1640-1
Brand: rocuronium bromide
Generic: rocuronium bromidePackage Facts
Identity
Package NDC
51662-1640-1
Digits Only
5166216401
Product NDC
51662-1640
Description
5 mL in 1 VIAL, MULTI-DOSE (51662-1640-1)
Marketing
Marketing Status
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": "0ffaf004-4d5b-3fd4-e063-6294a90a1a63", "openfda": {"unii": ["I65MW4OFHZ"], "rxcui": ["1234995"], "spl_set_id": ["074abb29-72d9-b09f-e063-6294a90af0a9"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "5 mL in 1 VIAL, MULTI-DOSE (51662-1640-1)", "package_ndc": "51662-1640-1", "marketing_start_date": "20230717"}], "brand_name": "ROCURONIUM BROMIDE", "product_id": "51662-1640_0ffaf004-4d5b-3fd4-e063-6294a90a1a63", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Neuromuscular Nondepolarizing Blockade [PE]", "Nondepolarizing Neuromuscular Blocker [EPC]"], "product_ndc": "51662-1640", "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": "ANDA205656", "marketing_category": "ANDA", "marketing_start_date": "20230717", "listing_expiration_date": "20261231"}