Atlas FDA

Water for Injection Sterile, USP

FDA premarket approval P100030/S009 · decided 2017-11-20

Approval details

PMA number
P100030
Supplement
S009
Supplement type
135 Review Track For 30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Water for Injection Sterile, USP
Generic name
Sealant, polymerizing
Applicant
Baxter Healthcare Corporation
Date received
2017-07-07
Decision date
2017-11-20
Days to decision
136 days
Decision code
APPR
Product code
NBE
Advisory committee
Cardiovascular
Expedited review
No
Location
Deerfield Lake, IL
Statement
Approval for an alternate supplier for the Sterile Water for Injection.

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