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Drug company (FDA labeler)

The J. Molner Company LLC

NDC labeler code: 83148

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

5Products (NDC)

Prescription medicines

FDA applications for these products

  • ANDA: Abbreviated New Drug Application: how a generic version is approved.
ApprovedApplicationMedicineSponsor
April 29, 2024ANDA218411 Lidocaine
LIDOCAINE HYDROCHLORIDE
The J Molner
September 17, 2020ANDA210223 Desmopressin acetate
DESMOPRESSIN ACETATE
Ubi
October 23, 2018ANDA209973 Desoximetasone
DESOXIMETASONE
The J Molner
November 21, 2017ANDA209556 Hydrocortisone butyrate
HYDROCORTISONE BUTYRATE
The J Molner
August 21, 2017ANDA209411 Clobetasol propionate
CLOBETASOL PROPIONATE (EMOLLIENT)
Beach Prods

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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