vecuronium bromide

Generic: vecuronium bromide

Labeler: hf acquisition co llc, dba healthfirst
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name vecuronium bromide
Generic Name vecuronium bromide
Labeler hf acquisition co llc, dba healthfirst
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

vecuronium bromide 10 mg/1

Manufacturer
HF Acquisition Co LLC, DBA HealthFirst

Identifiers & Regulatory

Product NDC 51662-1547
Product ID 51662-1547_1203bbfe-c55b-1bcb-e063-6394a90a6577
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206670
Listing Expiration 2026-12-31
Marketing Start 2022-07-31

Pharmacologic Class

Classes
neuromuscular nondepolarizing blockade [pe] nondepolarizing neuromuscular blocker [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621547
Hyphenated Format 51662-1547

Supplemental Identifiers

RxCUI
859437
UPC
0355150235018
UNII
7E4PHP5N1D

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name vecuronium bromide (source: ndc)
Generic Name vecuronium bromide (source: ndc)
Application Number ANDA206670 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (51662-1547-1)
source: ndc

Packages (1)

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

Ingredients (1)

vecuronium bromide (10 mg/1)

Linked Drug Pages (1)

VECURONIUM BROMIDE ndc-match (0.9)

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"}