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Drug company (FDA labeler)

Carlsbad Technology, Inc.

NDC labeler code: 61442

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

29Products (NDC)

Prescription medicines

FDA applications for these products

  • ANDA: Abbreviated New Drug Application: how a generic version is approved.
ApprovedApplicationMedicineSponsor
November 10, 2021ANDA208195 Entecavir
ENTECAVIR
Yung Shin Pharm
April 3, 2020ANDA212947 Memantine hydrochloride
MEMANTINE HYDROCHLORIDE
Pharmobedient
April 29, 2019ANDA204800 Felodipine
FELODIPINE
Yung Shin Pharm
August 16, 2017ANDA206261 Acyclovir
ACYCLOVIR
Carlsbad
September 22, 2009ANDA077911 Glimepiride
GLIMEPIRIDE
Carlsbad
December 7, 2006ANDA077918 Meloxicam
MELOXICAM
Yung Shin Pharm
June 9, 2004ANDA076126 Ciprofloxacin
CIPROFLOXACIN, CIPROFLOXACIN HYDROCHLORIDE
Carlsbad
January 22, 2004ANDA065146 Cefaclor
CEFACLOR
Yung Shin Pharm
June 5, 2002ANDA075991 Lovastatin
LOVASTATIN
Carlsbad
April 16, 2001ANDA075805 Famotidine
FAMOTIDINE
Carlsbad
April 30, 1999ANDA075382 Acyclovir
ACYCLOVIR
Carlsbad
November 13, 1998ANDA075185 Diclofenac
DICLOFENAC SODIUM
Carlsbad

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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