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Drug company (FDA labeler)

Bostal LLC

NDC labeler code: 35561

What is a labeler?

The company whose name is on the package and in the FDA’s National Drug Code (NDC) Directory. It may make the medicine itself or sell medicine made by another company. The first part of every NDC code identifies the labeler.

Official FDA data only

Products, approvals and recalls come from the FDA (NDC Directory, Drugs@FDA, enforcement reports). Recalls are linked to this company by the NDC labeler code on the recalled product.

Questions about your medicine: ask your doctor or pharmacist. In an emergency, call 911.

At a glance

22Products (NDC)

Prescription medicines

FDA applications for these products

  • ANDA: Abbreviated New Drug Application: how a generic version is approved.
ApprovedApplicationMedicineSponsor
March 31, 2022ANDA215591 Carbamazepine
CARBAMAZEPINE
Zhejiang Jiuzhou
February 10, 2021ANDA208476 Fenofibrate
FENOFIBRATE
Bostal
October 27, 2020ANDA208824 Tadalafil
TADALAFIL
Hangzhou Binjiang
June 12, 2020ANDA208494 Sildenafil
SILDENAFIL CITRATE
Reyoung
May 20, 2019ANDA210281 Solifenacin succinate
SOLIFENACIN SUCCINATE
Bostal
December 19, 2017ANDA207803 Fenofibrate
FENOFIBRATE
Bostal
November 16, 2017ANDA207805 Fenofibrate
FENOFIBRATE (MICRONIZED)
Reyoung
October 21, 2011ANDA200958 Methocarbamol
METHOCARBAMOL
Bostal

The sponsor is the company that holds the FDA application; it can differ from the labeler.

Recall timeline

No recall of these products (by NDC code) appears in the FDA enforcement reports.

Sources

  1. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  2. Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026

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