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Drug company (FDA labeler)

Sentiss Pharmaceuticals LLC

NDC labeler code: 70244

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

6Products (NDC)

FDA applications for these products

  • ANDA: Abbreviated New Drug Application: how a generic version is approved.
ApprovedApplicationMedicineSponsor
June 9, 2023ANDA215768 Ciprofloxacin and dexamethasone
CIPROFLOXACIN AND DEXAMETHASONE
Sentiss
April 12, 2023ANDA215933 Loteprednol etabonate
LOTEPREDNOL ETABONATE
Sentiss
February 10, 2021ANDA212080 Loteprednol etabonate
LOTEPREDNOL ETABONATE
Sentiss
April 17, 2019ANDA207609 Loteprednol etabonate
LOTEPREDNOL ETABONATE
Sentiss
February 12, 2003ANDA040433 Lidocaine
LIDOCAINE HYDROCHLORIDE
Sentiss
July 18, 1996ANDA064030 Erythromycin
ERYTHROMYCIN
Sentiss

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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