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MedsAcross

Medicine

Lanreotide 60 mg/0.2 mL injection

Lanreotide · Subcutaneous
Available on requestPrescription onlyUS FDA Cold chainGeneric name

Lanreotide 60 mg/0.2 mL injection is a generic prescription medicine for subcutaneous use, made by 2 labelers, with its source record on the US FDA register. It is available on request for export supply from India to licensed hospitals, importers and physicians. It ships in a temperature-controlled cold chain.

Availability

Available on request

Export supply from India to licensed buyers

Typical lead time

On request

Counted from payment and complete documents

Shipping

Cold chain

Store Lanreotide Injection in the refrigerator at 2°C to 8°C (36°F to 46°F)…

Key facts

Active ingredient (INN)
Lanreotide
Brand
Sold under the generic name
Strength
60 mg/0.2 mL
Dosage form
Injection
Route
Subcutaneous
Packs
1 syringe of 0.2 mL, 1 pouch of 0.2 mL
Manufacturers
CiplaIndiaExelan Pharmaceuticals
Origin register
US FDA, United States
Storage
Store Lanreotide Injection in the refrigerator at 2°C to 8°C (36°F to 46°F). Protect from light. Store in the original package.
Cold chain
Yes, shipped temperature controlled
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
H01CB03 Lanreotide
HS code (indicative)
3004.39Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
24 December 2021
Identifiers
RxCUI 749811, 749814, 749817DailyMed set ID eec3c37e-83a7-4195-bccf-cd5973459eef, 2892b4c3-0329-4d29-97ff-3b45283bbab1, 11da176a-99bc-4ada-8b3f-6bd2b37a6313NDC 76282-718, 69097-907, 69097-880Application ANDA217193, NDA215395

Record updated 12 November 2026

Documents available

Documents that can be provided with this medicine. Your regulator may ask for more, and the quote lists the full set.

No document list is recorded for this medicine yet. Tell us which documents your regulator needs (for example a CoA, COPP or GMP certificate) when you request a quote.

Packs

Packs from every labeler of this generic presentation.

PackCodeLabelerMarketed since
1 syringe in 1 carton / .2 mL in 1 syringe69097-880-67CiplaIndia24 December 2021
1 pouch in 1 carton / 1 syringe in 1 pouch / .2 mL in 1 syringe69097-907-67CiplaIndia30 May 2025
1 pouch in 1 carton / 1 syringe in 1 pouch / .2 mL in 1 syringe76282-718-67Exelan Pharmaceuticals30 May 2025

Status by register

Where this medicine is registered, from the source record and the regulator data we hold. Ask us about a country that is not listed.

RegisterStatusSource
US FDAListed, marketedSource record for this pageChecked 12 November 2026
US FDAFirst approved 30 August 2007Drugs@FDA
EU (EMA)Not recorded—
India (CDSCO)Not yet confirmed against CDSCO approval lists—
United StatesRegisteredUS FDA (NDC directory, openFDA)Checked 12 November 2026

Import route

Pick the destination country to see the legal import route, who applies and typical timelines, from our import guide for that country.

Import guides are available for 25 countries. Pick one to see its route summary.

BrazilColombiaEgyptEthiopiaGhanaIraqKazakhstanKenyaAll import guides

Alternatives

Other makers and brands of Lanreotide 60 mg/0.2 mL injection.

Compare 1

Other strengths and forms of Lanreotide

Clinical summary

Lanreotide is a somatostatin analog indicated for the long-term treatment of acromegalic patients who have had an inadequate response to or cannot be treated with surgery and/or radiotherapy, among other approved uses. MedsAcross supplies Lanreotide for export from India to licensed hospitals, importers and physicians acting for named patients, with the documents each country requires.

Information from the US FDA prescribing information, retrieved 12 November 2026. Not yet medically reviewed.How we review

Read about Lanreotide

For healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.

Data sources

Need Lanreotide 60 mg/0.2 mL injection for your hospital or patient?

Send one request with the destination country and quantity. We confirm availability, lead time and the documents your regulator needs.