NDC 0591-2136-80 - Propofol

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

0591-2136

Requested NDC

0591-2136-80

Package NDCs from labels

0591-2136-55, 0591-2136-51, 0591-2136-57, 0591-2136-68, 0591-2136-80, 0591-2136-95

Manufacturer

Actavis Pharma, Inc.

Effective date

2023-05-30

Current FDA listing

Not matched in FDA.report NDC product tables