vecuronium bromide
Generic: vecuronium bromide
Labeler: fresenius kabi usa, llcDrug Facts
Product Profile
Brand Name
vecuronium bromide
Generic Name
vecuronium bromide
Labeler
fresenius kabi usa, llc
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
vecuronium bromide 1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
63323-781
Product ID
63323-781_ef0a4c9f-a65e-48dd-b625-eb76a18905f2
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA205390
Listing Expiration
2026-12-31
Marketing Start
2016-06-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63323781
Hyphenated Format
63323-781
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
ANDA205390 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/mL
Packaging
- 10 VIAL in 1 CARTON (63323-781-10) / 10 mL in 1 VIAL (63323-781-21)
Packages (1)
Ingredients (1)
Linked Drug Pages (2)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "ef0a4c9f-a65e-48dd-b625-eb76a18905f2", "openfda": {"unii": ["7E4PHP5N1D"], "rxcui": ["859437"], "spl_set_id": ["d3163bdf-f163-41b5-a38a-3cd6fc1a50ba"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (63323-781-10) / 10 mL in 1 VIAL (63323-781-21)", "package_ndc": "63323-781-10", "marketing_start_date": "20160630"}], "brand_name": "Vecuronium Bromide", "product_id": "63323-781_ef0a4c9f-a65e-48dd-b625-eb76a18905f2", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Neuromuscular Nondepolarizing Blockade [PE]", "Nondepolarizing Neuromuscular Blocker [EPC]"], "product_ndc": "63323-781", "generic_name": "Vecuronium Bromide", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vecuronium Bromide", "active_ingredients": [{"name": "VECURONIUM BROMIDE", "strength": "1 mg/mL"}], "application_number": "ANDA205390", "marketing_category": "ANDA", "marketing_start_date": "20160630", "listing_expiration_date": "20261231"}