QKit Procedure Tray
QKit
Approved
Approval ID
6d061538-7a4e-4af2-a4a6-a9b010c092f6
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Aug 16, 2016
Manufacturers
FDA
CooperSurgical, Inc.
DUNS: 801895244
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
lidocaine hydrochloride, epinephrine bitartrate, ferric subsulfate aqueous, iodine and potassium iodide
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code59365-9074
Product Classification
G
Generic Name
lidocaine hydrochloride, epinephrine bitartrate, ferric subsulfate aqueous, iodine and potassium iodide
Product Specifications
Effective DateApril 15, 2020
FDA Product Classification