vecuronium bromide
Generic: vecuronium bromide
Labeler: meitheal pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
vecuronium bromide
Generic Name
vecuronium bromide
Labeler
meitheal pharmaceuticals inc.
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
vecuronium bromide 10 mg/10mL
Manufacturer
Identifiers & Regulatory
Product NDC
71288-744
Product ID
71288-744_ef72e810-c31d-4c0a-8a7f-b1cfd8ac15ec
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA074688
Listing Expiration
2026-12-31
Marketing Start
2025-07-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71288744
Hyphenated Format
71288-744
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
ANDA074688 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/10mL
Packaging
- 10 VIAL, SINGLE-USE in 1 CARTON (71288-744-11) / 10 mL in 1 VIAL, SINGLE-USE (71288-744-10)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "ef72e810-c31d-4c0a-8a7f-b1cfd8ac15ec", "openfda": {"unii": ["7E4PHP5N1D"], "rxcui": ["859437"], "spl_set_id": ["53653418-0464-4cd2-a987-3d31be36098f"], "manufacturer_name": ["Meitheal Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-USE in 1 CARTON (71288-744-11) / 10 mL in 1 VIAL, SINGLE-USE (71288-744-10)", "package_ndc": "71288-744-11", "marketing_start_date": "20250701"}], "brand_name": "Vecuronium Bromide", "product_id": "71288-744_ef72e810-c31d-4c0a-8a7f-b1cfd8ac15ec", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Neuromuscular Nondepolarizing Blockade [PE]", "Nondepolarizing Neuromuscular Blocker [EPC]"], "product_ndc": "71288-744", "generic_name": "Vecuronium Bromide", "labeler_name": "Meitheal Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vecuronium Bromide", "active_ingredients": [{"name": "VECURONIUM BROMIDE", "strength": "10 mg/10mL"}], "application_number": "ANDA074688", "marketing_category": "ANDA", "marketing_start_date": "20250701", "listing_expiration_date": "20261231"}