HAISCO: New drug application for CYPSEDO

HAISCO: New drug application for CYPSEDO. Dated 159 days ago, it serves as a historical benchmark. Score 55/100. As of 2026-11-03, from openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration).

Data as of · Compiled by Zalwin from openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration)

Free preview: all 7 published fields of this record are shown below. Locked: 499 related FdaApprovalPulse records and the 4-column CSV export.

FieldValue
SponsorHAISCO
ProductCYPSEDO
Generic / ingredientCIPEPOFOL
ApprovalNew drug application (NDA)
ApplicationNDA220482
Decided2026-05-29
Panel / classEMULSION, INTRAVENOUS
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  • Source agency: openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration)
  • Record date: 2026-05-29
  • Data refreshed: 2026-11-03
  • Refunds on request within 14 days

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LIVE PUBLIC DATA Source: openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration) · Last refreshed: Tue, 03 Nov 2026 05:14:00 GMT

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55 / 100 Score

  • A new product launch.

What is the FdaApprovalPulse record for HAISCO?

The FDA approved CYPSEDO (NDA220482) for HAISCO on 2026-05-29: new drug application (NDA).

How does HAISCO compare to other FdaApprovalPulse records?

It is 159 days old; check the official source for later updates before acting.

HAISCO vs. top 3 peers

OrganizationRecord date
HAISCO2026-05-29
GLAXOSMITHKLINE LLC2026-10-20
FRESENIUS MEDCL CARE2026-10-19
FRESENIUS MEDCL CARE2026-10-19

Related records

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From openFDA (PMA and Drugs@FDA). openFDA can lag FDA decisions by days to weeks. Drug supplement types follow the FDA submission class (labeling and REMS, manufacturing/CMC, efficacy, other). Company and product level only. Verify on FDA databases before relying on an approval.

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