Exeltis Pharma Mexico SA de CV
FDA import alert and refusal historyTultitlan, MexicoFEI 3021173860
Recorded by FDA as EXELTIS PHARMA MEXICO SA DE CV
As of October 26, 2026, Exeltis Pharma Mexico SA de CV is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines between November 14, 2024 and May 27, 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
- Folic acid (vitamin) · UNAPPROVED
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Exeltis Pharma Mexico SA de CV
3 records, newest first. Each line links to the FDA page it came from.
2025
- Import refusalSource
Refused, 2 lines in one entry: Folic acid (vitamin)UNAPPROVEDEntry 799-7024858-0Show 2 linesHide lines
- Refused, Folic acid (vitamin)UNAPPROVEDEntry 799-7024858-0Source
- Refused, Folic acid (vitamin)UNAPPROVEDEntry 799-7024858-0Source
2024
- Import refusalRefused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry 799-4049940-4Source
Refusal charges, in plain English
- UNAPPROVED3 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 Exeltis Pharma Mexico SA de CV
- Is Exeltis Pharma Mexico SA de CV on an FDA import alert?
- No listing for Exeltis Pharma Mexico SA de CV appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Mexico page.
- Has FDA refused shipments from Exeltis Pharma Mexico SA de CV?
- Yes. FDA refused 3 shipment lines from Exeltis Pharma Mexico SA de CV between November 14, 2024 and May 27, 2025. The most recent, on May 27, 2025, was folic acid (vitamin), charged as UNAPPROVED (unapproved new drug).
- Why did FDA refuse Exeltis Pharma Mexico SA de CV's shipments?
- The most frequent charge is UNAPPROVED (unapproved new drug, 3 lines).
- What is Exeltis Pharma Mexico SA de CV's FEI number?
- Exeltis Pharma Mexico SA de CV's FDA Establishment Identifier (FEI) is 3021173860.
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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.