vecuronium bromide
Generic: vecuronium bromide
Labeler: hikma pharmaceuticals usa inc.Drug Facts
Product Profile
Brand Name
vecuronium bromide
Generic Name
vecuronium bromide
Labeler
hikma pharmaceuticals usa inc.
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
vecuronium bromide 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0143-9232
Product ID
0143-9232_447053f5-3015-4770-9e16-a5c82513249d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203725
Listing Expiration
2027-12-31
Marketing Start
2019-08-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
01439232
Hyphenated Format
0143-9232
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
ANDA203725 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 10 VIAL in 1 CARTON (0143-9232-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9232-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "447053f5-3015-4770-9e16-a5c82513249d", "openfda": {"unii": ["7E4PHP5N1D"], "rxcui": ["859437"], "spl_set_id": ["dceeec01-2910-4489-8d70-9c0c711d17ab"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (0143-9232-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9232-01)", "package_ndc": "0143-9232-10", "marketing_start_date": "20190801"}], "brand_name": "Vecuronium Bromide", "product_id": "0143-9232_447053f5-3015-4770-9e16-a5c82513249d", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Neuromuscular Nondepolarizing Blockade [PE]", "Nondepolarizing Neuromuscular Blocker [EPC]"], "product_ndc": "0143-9232", "generic_name": "Vecuronium Bromide", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vecuronium Bromide", "active_ingredients": [{"name": "VECURONIUM BROMIDE", "strength": "20 mg/1"}], "application_number": "ANDA203725", "marketing_category": "ANDA", "marketing_start_date": "20190801", "listing_expiration_date": "20271231"}