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Drug company (FDA labeler)

HEC Pharm USA Inc.

NDC labeler code: 72303

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)

FDA applications for these products

  • ANDA: Abbreviated New Drug Application: how a generic version is approved.
ApprovedApplicationMedicineSponsor
January 5, 2022ANDA213594 Oseltamivir phosphate
OSELTAMIVIR PHOSPHATE
Sunshine
June 11, 2020ANDA213032 Sildenafil
SILDENAFIL CITRATE
Sunshine
June 2, 2020ANDA213069 Febuxostat
FEBUXOSTAT
Sunshine
April 13, 2020ANDA213346 Solifenacin succinate
SOLIFENACIN SUCCINATE
Sunshine
April 1, 2020ANDA210667 Rosuvastatin
ROSUVASTATIN CALCIUM
Sunshine
March 26, 2019ANDA211335 Tadalafil
TADALAFIL
Sunshine
February 22, 2019ANDA211049 Olmesartan medoxomil
OLMESARTAN MEDOXOMIL
Sunshine
November 19, 2018ANDA206238 Olanzapine
OLANZAPINE
Sunshine
July 3, 2018ANDA208146 Olanzapine
OLANZAPINE
Hec Pharm

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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