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VECURONIUM BROMIDE Recall D-1079-2022

Description: Vecuronium Bromide for Injection, 10 mg (1mg/ mL) vial, 10-count box, Rx only, MFG: Teva Pharma USA, NDC 0703-2914-03

VECURONIUM BROMIDE Recall D-1079-2022 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberD-1079-2022
Event ID89646
BrandVECURONIUM BROMIDE
Generic NameVECURONIUM BROMIDE
ManufacturerVECURONIUM BROMIDE
Original Package?1
Active SubstanceVECURONIUM BROMIDE
Drug RouteINTRAVENOUS
DistributionUSA nationwide.
Quantity20 cartons/10 vials each
Recall ReasoncGMP deviations: Temperature abuse
Drug ClassificationClass II
Drug Code Info20220615
Product NDC0703-2914 0703-2925
Recall Initiation Date20220413
Report Date20220615
Classification Date20220609
Address9954 Maryland DriveDeep Run Iii Ste. 4000
Richmond, VA 23233
United States
Recalling FirmMckesson Medical-Surgical Inc. Corporate Office
Initial Notification Letter
Unique Ingredient Identifier7E4PHP5N1D
Drug Application NumberANDA074688
Structured Product Labeling (SPL ID)7525d8ef-dedb-42b0-85d4-0e596af4aec7
Structured Product Labeling (SPL Set ID)eaa404d1-68a9-4fac-b3f3-b444a20df120
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