NDC 83854-018-01 - 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

83854-018

Requested NDC

83854-018-01

Package NDCs from labels

83854-018-01, 83854-018-10, 83854-018-16, 83854-018-14, 83854-018-15

Manufacturer

Anthea Pharma Private Limited

Effective date

2026-09-29

Current FDA listing

Not matched in FDA.report NDC product tables