vecuronium bromide
Generic: vecuronium bromide
Labeler: eugia us llcDrug Facts
Product Profile
Brand Name
vecuronium bromide
Generic Name
vecuronium bromide
Labeler
eugia us llc
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
vecuronium bromide 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
55150-236
Product ID
55150-236_26368338-338e-4438-8fc7-366e8e6f9bbb
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA206670
Listing Expiration
2026-12-31
Marketing Start
2018-12-20
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
55150236
Hyphenated Format
55150-236
Supplemental Identifiers
RxCUI
UPC
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
ANDA206670 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 10 VIAL in 1 CARTON (55150-236-20) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (55150-236-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (2)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "26368338-338e-4438-8fc7-366e8e6f9bbb", "openfda": {"upc": ["0355150236015", "0355150235100", "0355150236206", "0355150235018"], "unii": ["7E4PHP5N1D"], "rxcui": ["859437"], "spl_set_id": ["86d81719-534c-4e50-ae39-d8b20e50dfad"], "manufacturer_name": ["Eugia US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (55150-236-20) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (55150-236-01)", "package_ndc": "55150-236-20", "marketing_start_date": "20181220"}], "brand_name": "VECURONIUM BROMIDE", "product_id": "55150-236_26368338-338e-4438-8fc7-366e8e6f9bbb", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Neuromuscular Nondepolarizing Blockade [PE]", "Nondepolarizing Neuromuscular Blocker [EPC]"], "product_ndc": "55150-236", "generic_name": "VECURONIUM BROMIDE", "labeler_name": "Eugia US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VECURONIUM BROMIDE", "active_ingredients": [{"name": "VECURONIUM BROMIDE", "strength": "20 mg/1"}], "application_number": "ANDA206670", "marketing_category": "ANDA", "marketing_start_date": "20181220", "listing_expiration_date": "20261231"}