Package 51662-1547-1

Brand: vecuronium bromide

Generic: vecuronium bromide
NDC Package

Package Facts

Identity

Package NDC 51662-1547-1
Digits Only 5166215471
Product NDC 51662-1547
Description

1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (51662-1547-1)

Marketing

Marketing Status
Marketed Since 2022-07-31
Brand vecuronium bromide
Generic vecuronium bromide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "1203bbfe-c55b-1bcb-e063-6394a90a6577", "openfda": {"upc": ["0355150235018"], "unii": ["7E4PHP5N1D"], "rxcui": ["859437"], "spl_set_id": ["e51c763e-2819-341f-e053-2995a90a0565"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (51662-1547-1)", "package_ndc": "51662-1547-1", "marketing_start_date": "20220731"}], "brand_name": "VECURONIUM BROMIDE", "product_id": "51662-1547_1203bbfe-c55b-1bcb-e063-6394a90a6577", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Neuromuscular Nondepolarizing Blockade [PE]", "Nondepolarizing Neuromuscular Blocker [EPC]"], "product_ndc": "51662-1547", "generic_name": "VECURONIUM BROMIDE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VECURONIUM BROMIDE", "active_ingredients": [{"name": "VECURONIUM BROMIDE", "strength": "10 mg/1"}], "application_number": "ANDA206670", "marketing_category": "ANDA", "marketing_start_date": "20220731", "listing_expiration_date": "20261231"}