FDA.reportPublic FDA data

NDC 10019-481 - Vecuronium Bromide

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
10019-481
Package NDCs from labels
10019-481-10, 10019-481-01
Manufacturer
Watson Laboratories, Inc.
Effective date
2007-06-25
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
VECURONIUM BROMIDE FOR INJECTION Rx onlyWatson Laboratories, Inc.2007-06-25HUMAN PRESCRIPTION DRUG LABELING

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10019-481-01Vecuronium Bromide10 in 1 CARTONINJECTION, POWDER, LYOPHILIZED,101
10019-481-10Vecuronium Bromide1 in 1 VIALINJECTION, POWDER, LYOPHILIZED,11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10019-481VECURONIUM BROMIDE (VECURONIUM BROMIDE) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [WATSON LABORATORIES, INC.]12 package rows20070706_A3DB901C-191C-472B-8BBC-5F12472C6D02.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
Vecuronium BromideACTIVE INGREDIENT7E4PHP5N1DVECURONIUM BROMIDE (VECURONIUM BROMIDE) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [WATSON LABORATORIES, INC.]1
Vecuronium cationACTIVE MOIETY5438723848VECURONIUM BROMIDE (VECURONIUM BROMIDE) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [WATSON LABORATORIES, INC.]1
Citric Acid AnhydrousINACTIVE INGREDIENTVECURONIUM BROMIDE (VECURONIUM BROMIDE) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [WATSON LABORATORIES, INC.]1
MannitolINACTIVE INGREDIENT3OWL53L36AVECURONIUM BROMIDE (VECURONIUM BROMIDE) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [WATSON LABORATORIES, INC.]1
Phosphoric AcidINACTIVE INGREDIENTE4GA8884NNVECURONIUM BROMIDE (VECURONIUM BROMIDE) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [WATSON LABORATORIES, INC.]1
Sodium HydroxideINACTIVE INGREDIENT55X04QC32IVECURONIUM BROMIDE (VECURONIUM BROMIDE) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [WATSON LABORATORIES, INC.]1
Sodium Phosphate Dibasic AnhydrousINACTIVE INGREDIENTVECURONIUM BROMIDE (VECURONIUM BROMIDE) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [WATSON LABORATORIES, INC.]1

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 ยท 12 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
VECURONIUM BROMIDEVECURONIUM BROMIDEHF Acquisition Co LLC, DBA HealthFirst582c7f44-b614-18df-e063-6294a90a74b62026-08-03Warnings, Adverse reactionsExact identifier
rxcui: 859437
vecuronium bromideVECURONIUM BROMIDESun Pharmaceutical Industries, Inc.a14da3ee-a731-4282-be9d-4074735174702026-07-24Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 859437
Vecuronium BromideVECURONIUM BROMIDEPhlow Corp.b012b1b1-9e59-4525-8f4d-dae98344d15f2026-03-19Warnings, Adverse reactionsExact identifier
rxcui: 859437
Vecuronium BromideVECURONIUM BROMIDEHikma Pharmaceuticals USA Inc.dceeec01-2910-4489-8d70-9c0c711d17ab2026-01-29Warnings, Adverse reactionsExact identifier
rxcui: 859437
Vecuronium BromideVECURONIUM BROMIDEMullan Pharmaceutical Inc.aa35d139-25c8-4802-b165-0db7d1c089132025-11-24Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 859437
Vecuronium BromideVECURONIUM BROMIDEMeitheal Pharmaceuticals Inc.53653418-0464-4cd2-a987-3d31be36098f2025-06-18Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 859437
VECURONIUM BROMIDEVECURONIUM BROMIDEEugia US LLC387b57ce-e50e-4e03-86d9-12638242bd362025-01-17Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 859437
Vecuronium BromideVECURONIUM BROMIDESagent Pharmaceuticalsdff452e8-71e7-437e-bed0-3e1bd9441bc62024-07-18Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 859437
VECURONIUM BROMIDEVECURONIUM BROMIDEHF Acquisition Co LLC, DBA HealthFirste51c763e-2819-341f-e053-2995a90a05652024-02-22Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 859437
VECURONIUM BROMIDEVECURONIUM BROMIDEEugia US LLC86d81719-534c-4e50-ae39-d8b20e50dfad2023-12-06Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 859437
VECURONIUM BROMIDEVECURONIUM BROMIDEMylan Institutional LLC96e69586-e9af-4b07-990f-12d93faa7edd2022-10-31Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 859437
Vecuronium BromideVECURONIUM BROMIDEGland Pharma Limited5ae91612-4f65-4e52-8901-c37010612eaf2018-07-16Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 859437

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.