Vecuronium Bromide

Product NDC
0409-1634
11-digit product format
004091634
Labeler code
0409
Product ID
0409-1634_a842348f-f29c-4387-9125-7cca44d69ae5
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Vecuronium Bromide
Dosage form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route
INTRAVENOUS
Labeler
Hospira, Inc.
Application
ANDA075164
Marketing category
ANDA
Marketing start
2006-03-03
Marketing end
2023-05-01
Substance
VECURONIUM BROMIDE
Active strength
1 mg/mL
Pharmacologic classes
Neuromuscular Nondepolarizing Blockade [PE], Nondepolarizing Neuromuscular Blocker [EPC]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0409-1634-01EA - Each0409-163483d45ff5-09ec-4059-8d0f-3d9ecd9e1aa612012-07-24
0409-1634-49EA - Each0409-1634d52ce2c0-f2f0-4191-8d0e-c70fb398c38112012-07-24
0409-1634-85EA - Each0409-1634c466fbcf-3943-45c8-b970-61906699fbaf12020-02-13

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0409-1634VECURONIUM BROMIDE INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [HOSPIRA, INC.]20Legacy NDC20240918_bd49ff83-5c84-436b-35bb-08cfd3182975.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0409-1634-010040916340110 VIAL in 1 CARTON (0409-1634-01) > 20 mL in 1 VIAL (0409-1634-85) 10 vial2006-03-032023-05-01NoNoCurrent