Tuton Pharmaceuticals
FDA import alert and refusal historyAhmedabad, IndiaFEI 3020377807
Recorded by FDA as TUTON PHARMACEUTICALS
As of October 26, 2026, Tuton Pharmaceuticals is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines between October 18, 2024 and July 8, 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 b2 (riboflavin) · UNAPPROVED
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Tuton Pharmaceuticals
2 records, newest first. Each line links to the FDA page it came from.
2025
- Import refusalRefused, Vitamin b2 (riboflavin)UNAPPROVEDEntry AEK-8554975-4Source
2024
- Import refusalRefused, Mecobalamin (vitamin)UNAPPROVEDEntry AEK-5791285-7Source
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 Tuton Pharmaceuticals
- Is Tuton Pharmaceuticals on an FDA import alert?
- No listing for Tuton Pharmaceuticals appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the India page.
- Has FDA refused shipments from Tuton Pharmaceuticals?
- Yes. FDA refused 2 shipment lines from Tuton Pharmaceuticals between October 18, 2024 and July 8, 2025. The most recent, on July 8, 2025, was vitamin b2 (riboflavin), charged as UNAPPROVED (unapproved new drug).
- Why did FDA refuse Tuton Pharmaceuticals's shipments?
- The most frequent charge is UNAPPROVED (unapproved new drug, 2 lines).
- What is Tuton Pharmaceuticals's FEI number?
- Tuton Pharmaceuticals's FDA Establishment Identifier (FEI) is 3020377807.
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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.