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Drug company (FDA labeler)

Phlow Corporation

NDC labeler code: 81565

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

4Products (NDC)

Prescription medicines

FDA applications for these products

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
  • ANDA: Abbreviated New Drug Application: how a generic version is approved.
ApprovedApplicationMedicineSponsor
December 29, 2008ANDA078651 Rocuronium bromide
ROCURONIUM BROMIDE
Fresenius Kabi USA
May 22, 1984NDA018902 Furosemide
FUROSEMIDE
Fresenius Kabi USA
September 6, 1977ANDA084916 Dexamethasone
DEXAMETHASONE SODIUM PHOSPHATE
Fresenius Kabi USA
February 22, 1972NDA017029 Heparin sodium
HEPARIN SODIUM, HEPARIN SODIUM 20,000 UNITS IN DEXTROSE 5%, HEPARIN SODIUM 25,000 UNITS IN DEXTROSE 5%
Fresenius Kabi USA

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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