SupplierRadar

Medpharma

FDA import alert and refusal historyGuatemala, GuatemalaFEI 3017178027

Recorded by FDA as MEDPHARMA

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Example subjectMedpharm added to Import Alert 16-129 (red list)

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As of October 25, 2026, Medpharma is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on September 23, 2025, most often for unapproved new drug (UNAPPROVED).

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
Not listed
Last import refusal
Vitamin c (ascorbic acid) · UNAPPROVED
Last warning letter
None found
Last inspection
None on record

Every FDA record for Medpharma

2 records, newest first. Each line links to the FDA page it came from.

2025

  1. Import refusal
    Refused, Vitamin c (ascorbic acid)UNAPPROVEDEntry AEK-7631380-6
    Source
  2. Import refusal
    Refused, Vitamin c (ascorbic acid)UNAPPROVEDEntry AEK-7483646-9
    Source

Refusal charges, in plain English

  • UNAPPROVED2 refused lines

    Unapproved new drug

    The product appeared to be a new drug within the meaning of section 201(p) of the FD&C Act without an approved New Drug Application. FDA can apply this charge to a food or supplement whose labeling presents it for drug uses.

Questions about Medpharma

Is Medpharma on an FDA import alert?
No listing for Medpharma appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Guatemala page.
Has FDA refused shipments from Medpharma?
Yes. FDA refused 2 shipment lines from Medpharma on September 23, 2025. The most recent, on September 23, 2025, was vitamin c (ascorbic acid), charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Medpharma's shipments?
The most frequent charge is UNAPPROVED (unapproved new drug, 2 lines).
What is Medpharma's FEI number?
Medpharma's FDA Establishment Identifier (FEI) is 3017178027.

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Example subjectMedpharm added to Import Alert 16-129 (red list)

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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.