Drogueria Luipharm
FDA import alert and refusal historyCiu, GuatemalaFEI 3039772599
Recorded by FDA as DROGUERIA LUIPHARM
As of October 26, 2026, Drogueria Luipharm is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines between February 10, 2026 and March 1, 2026, 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 Drogueria Luipharm
2 records, newest first. Each line links to the FDA page it came from.
2026
- Import refusalRefused, Vitamin c (ascorbic acid)UNAPPROVEDEntry AEK-9452155-4Source
- Import refusalRefused, Vitamin c (ascorbic acid)UNAPPROVEDEntry AEK-9281476-1Source
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 Drogueria Luipharm
- Is Drogueria Luipharm on an FDA import alert?
- No listing for Drogueria Luipharm appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Guatemala page.
- Has FDA refused shipments from Drogueria Luipharm?
- Yes. FDA refused 2 shipment lines from Drogueria Luipharm between February 10, 2026 and March 1, 2026. The most recent, on March 1, 2026, was vitamin c (ascorbic acid), charged as UNAPPROVED (unapproved new drug).
- Why did FDA refuse Drogueria Luipharm's shipments?
- The most frequent charge is UNAPPROVED (unapproved new drug, 2 lines).
- What is Drogueria Luipharm's FEI number?
- Drogueria Luipharm's FDA Establishment Identifier (FEI) is 3039772599.
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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.