vecuronium bromide
Generic: vecuronium bromide
Labeler: sagent pharmaceuticalsDrug Facts
Product Profile
Brand Name
vecuronium bromide
Generic Name
vecuronium bromide
Labeler
sagent pharmaceuticals
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
vecuronium bromide 1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
25021-686
Product ID
25021-686_16c6cf89-dd59-4d0f-a006-fe0d0bc669d9
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA205390
Listing Expiration
2026-12-31
Marketing Start
2024-07-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
25021686
Hyphenated Format
25021-686
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 (25021-686-20) / 20 mL in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "16c6cf89-dd59-4d0f-a006-fe0d0bc669d9", "openfda": {"unii": ["7E4PHP5N1D"], "rxcui": ["859437"], "spl_set_id": ["dff452e8-71e7-437e-bed0-3e1bd9441bc6"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (25021-686-20) / 20 mL in 1 VIAL", "package_ndc": "25021-686-20", "marketing_start_date": "20240701"}], "brand_name": "Vecuronium Bromide", "product_id": "25021-686_16c6cf89-dd59-4d0f-a006-fe0d0bc669d9", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Neuromuscular Nondepolarizing Blockade [PE]", "Nondepolarizing Neuromuscular Blocker [EPC]"], "product_ndc": "25021-686", "generic_name": "Vecuronium Bromide", "labeler_name": "Sagent Pharmaceuticals", "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": "20240701", "listing_expiration_date": "20261231"}