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US FDA source recordAL · Approval Letter

ARGATROBAN IN SODIUM CHLORIDE — FDA Approval Letter (NDA 022485)

Issued to PLANO PHARMS. Application is approved as submitted.

Posted by FDA

September 29, 2026

Application

NDA 505b1 • 022485

Product

ARGATROBAN IN SODIUM CHLORIDE

Company

PLANO PHARMS

Stage

Final Decision

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What did FDA decide for ARGATROBAN IN SODIUM CHLORIDE?

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Source facts

FDA posted an approval letter for ARGATROBAN IN SODIUM CHLORIDE on 2026-09-29. This is the document posting date; consult the signed letter for the decision date. The source metadata identifies NDA 022485 as a supplement. Review the exact FDA letter for the approved conditions and labeling.

Key details in this letter

  • 1FDA action: approval.
  • 2Application: NDA 022485.
  • 3Submission: supplement.
  • 4Sponsor: PLANO PHARMS.

Suggested next step

Review the exact FDA letter for approved conditions, labeling, and postmarketing requirements.

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Built from structured FDA metadata and deterministic source-text signals. Topic matches are navigation aids, not legal or regulatory conclusions. Verify material decisions against the original FDA document.

FDAPDFUpdated Oct 8, 2026

FDA source document

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Common questions about the ARGATROBAN IN SODIUM CHLORIDE approval letter

Is ARGATROBAN IN SODIUM CHLORIDE FDA approved?

This letter documents an FDA approval action: FDA approved NDA 022485 for ARGATROBAN IN SODIUM CHLORIDE, sponsored by PLANO PHARMS,. Product may be marketed. Verify current status and labeling in the source letter, since later FDA actions can change them.

What is NDA 022485?

NDA 022485 is the application under which FDA issued this approval letter for ARGATROBAN IN SODIUM CHLORIDE to PLANO PHARMS. FDA posted the letter on September 29, 2026; the posting date is not the decision date.

What happens after an FDA approval letter?

The sponsor may market the product in line with the approved labeling. Approval letters typically set post-approval obligations: submitting final content of labeling, meeting any postmarketing requirements or commitments listed in the letter, updating Orange Book patent information within 30 days for NDAs, and ongoing annual reporting under 21 CFR 314.81.