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Drug company (FDA labeler)

Milla Pharmaceuticals Inc.

Name in FDA records: MILLA PHARMACEUTICALS INC.

NDC labeler code: 71357

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

11Products (NDC)

FDA applications for these products

  • ANDA: Abbreviated New Drug Application: how a generic version is approved.
ApprovedApplicationMedicineSponsor
July 6, 2026ANDA219089 Sodium bicarbonate
SODIUM BICARBONATE
Milla Pharms
December 31, 2024ANDA213116 Tromethamine
TROMETHAMINE
Milla Pharms
May 4, 2021ANDA214805 Sodium acetate
SODIUM ACETATE
Milla Pharms
January 7, 2020ANDA212046 Dihydroergotamine mesylate
DIHYDROERGOTAMINE MESYLATE
Milla Pharms
July 17, 2019ANDA212676 Tranexamic acid
TRANEXAMIC ACID
Milla Pharms
January 13, 2017ANDA207848 Piperacillin and tazobactam
PIPERACILLIN AND TAZOBACTAM
Milla Pharms

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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