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Brand-name prescription medicine

Langlara

Generic name: Insulin glargine

FDA application holder: Sunshine Lake Pharma Co Ltd

Official data, not advice

Everything here comes from the U.S. Food and Drug Administration (FDA): the NDC Directory, Drugs@FDA, the official labels and recall reports; pharmacy costs come from the Centers for Medicare & Medicaid Services (CMS). Each fact shows its source and date.

This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or switch any medicine, including a switch between a brand and a generic.

In an emergency, call 911. If someone may have taken too much of a medicine, call Poison Help: 1‑800‑222‑1222.

Quick answers

What is Langlara?
Langlara is a brand name of Insulin glargine, a prescription medicine. The FDA NDC Directory lists 1 Langlara product in 1 strength and form.
Who makes Langlara?
Sunshine Lake Pharma Co Ltd holds the FDA application for Langlara (BLA761412, approved April 29, 2026).
Is there a generic or store brand of Langlara?
Yes. The FDA NDC Directory lists 15 other products with the same active ingredients, strength and form as a Langlara product. Ask your pharmacist whether one is right for you.
Has Langlara been recalled?
No recall linked to Langlara products (by their NDC code or label) appears in the FDA enforcement reports we use.

What Langlara is

Each Langlara product as listed in the FDA NDC Directory, by active ingredient, strength and form, with its official label. “Same medicine, other names” counts the other products with exactly the same active ingredients, strength and form (generic versions, store brands and other brands); inactive ingredients can differ.

Insulin glargine · prescription medicine

Strength and formProduct namesSame medicine, other namesLabel
insulin glargine 100 units/mL
injection, solution (subcutaneous)
Langlara 15 products, 6 companies —

Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Insulin glargine →

FDA approval

  • BLA: Biologics License Application: how a biologic medicine (made from living cells) is approved.
FDA applications of Langlara products (Drugs@FDA)
ApplicationHolderFirst approvedProducts
BLA761412Sunshine Lake Pharma Co LtdApril 29, 20261

Companies that list Langlara

The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Langlara products.

Recalls

No recall linked to Langlara products (by their NDC code or label) 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 labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  4. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
  5. NADAC (National Average Drug Acquisition Cost) 2026 — Centers for Medicare & Medicaid Services (CMS), data.medicaid.gov, list of November 4, 2026, retrieved November 7, 2026

Which names get a brand page: a name the NDC Directory lists for a medicine, held by one company (the FDA application holder, or the company named on most of its products), that is not just a description, and that is not the only product of its medicine.

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