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Medicine

Liraglutide 18 mg/3 mL injection

Liraglutide · Subcutaneous
Available on requestPrescription onlyUS FDA Cold chainGeneric name

Liraglutide 18 mg/3 mL injection is a generic prescription medicine for subcutaneous use, made by 10 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

Prior to first use, liraglutide injection should be stored in a refrigerator…

Key facts

Active ingredient (INN)
Liraglutide
Brand
Sold under the generic name
Strength
18 mg/3 mL
Dosage form
Injection
Route
Subcutaneous
Packs
2 syringes of 3 mL, 3 syringes of 3 mL, 5 syringes of 3 mL and 25 more
Manufacturers
BioconIndiaCiplaIndiaOrbicular Pharmaceutical TechnologiesIndiaLupinIndiaHybio Pharmaceutical Co., Ltd. (Pingshan Factory)Teva PharmaceuticalsA-S Medication SolutionsHikma PharmaceuticalsMeitheal PharmaceuticalsNorthStar Rx
Origin register
US FDA, United States
Storage
Prior to first use, liraglutide injection should be stored in a refrigerator between 36ºF to 46ºF (2ºC to 8ºC). Do not store in the freezer or directly adjacent to the refrigerator cooling element. Do not freeze liraglutide injection and do not use liraglutide injection if it has been frozen.
Cold chain
Yes, shipped temperature controlled
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
A10BJ02 Liraglutide
HS code (indicative)
3004.39Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
21 June 2024
Identifiers
RxCUI 897122, 2735350DailyMed set ID 783c4a66-ba1f-4ee6-9024-c557a945a88c, 0b898330-eca1-f60a-71d2-b91716e336ed, 0efc3a89-211a-4496-baab-e8265e07de2b +14NDC 50090-8145, 70377-095, 71288-563 +12Application ANDA217590, ANDA217063, ANDA218115 +6

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
2 syringe, plastic in 1 carton / 3 mL in 1 syringe, plastic70377-094-52BioconIndia25 April 2026
3 syringe, plastic in 1 carton / 3 mL in 1 syringe, plastic70377-094-53BioconIndia25 April 2026
3 syringe, plastic in 1 carton / 3 mL in 1 syringe, plastic70377-095-52BioconIndia27 March 2026
5 syringe, plastic in 1 carton / 3 mL in 1 syringe, plastic70377-095-53BioconIndia27 March 2026
5 syringe, plastic in 1 carton / 3 mL in 1 syringe, plastic69097-910-55CiplaIndia25 February 2026
3 syringe, plastic in 1 carton / 3 mL in 1 syringe, plastic69097-910-68CiplaIndia25 February 2026
2 syringe, plastic in 1 carton / 3 mL in 1 syringe, plastic69097-920-67CiplaIndia22 January 2026
3 syringe, plastic in 1 carton / 3 mL in 1 syringe, plastic69097-920-68CiplaIndia22 January 2026
3 syringe, plastic in 1 carton / 3 mL in 1 syringe, plastic81607-018-01Orbicular Pharmaceutical TechnologiesIndia21 January 2026
2 syringe, plastic in 1 carton / 3 mL in 1 syringe, plastic81607-018-02Orbicular Pharmaceutical TechnologiesIndia21 January 2026
3 syringe, plastic in 1 carton / 3 mL in 1 syringe, plastic81607-019-01Orbicular Pharmaceutical TechnologiesIndia26 February 2026
5 syringe, plastic in 1 carton / 3 mL in 1 syringe, plastic81607-019-02Orbicular Pharmaceutical TechnologiesIndia26 February 2026
2 syringe, plastic in 1 carton / 3 mL in 1 syringe, plastic70748-346-02LupinIndia2 October 2025
3 syringe, plastic in 1 carton / 3 mL in 1 syringe, plastic70748-346-03LupinIndia2 October 2025
3 mL in 1 syringe, plastic14403-3400-1Hybio Pharmaceutical Co., Ltd. (Pingshan Factory)21 June 2024
2 syringe, plastic in 1 carton / 3 mL in 1 syringe, plastic14403-3400-2Hybio Pharmaceutical Co., Ltd. (Pingshan Factory)24 December 2024
3 syringe, plastic in 1 carton / 3 mL in 1 syringe, plastic14403-3400-3Hybio Pharmaceutical Co., Ltd. (Pingshan Factory)24 December 2024
2 syringe, plastic in 1 carton / 3 mL in 1 syringe, plastic0480-3667-20Teva Pharmaceuticals24 June 2024
3 syringe, plastic in 1 carton / 3 mL in 1 syringe, plastic0480-3667-22Teva Pharmaceuticals24 June 2024
5 syringe, plastic in 1 carton / 3 mL in 1 syringe, plastic0480-7250-46Teva Pharmaceuticals28 August 2025
2 syringe, plastic in 1 carton / 3 mL in 1 syringe, plastic0143-9144-02Hikma Pharmaceuticals24 December 2024
3 syringe, plastic in 1 carton / 3 mL in 1 syringe, plastic0143-9144-03Hikma Pharmaceuticals24 December 2024
3 syringe, plastic in 1 carton / 3 mL in 1 syringe, plastic71288-563-84Meitheal Pharmaceuticals2 April 2025
2 syringe, plastic in 1 carton / 3 mL in 1 syringe, plastic71288-563-85Meitheal Pharmaceuticals2 April 2025
3 syringe, plastic in 1 carton / 3 mL in 1 syringe, plastic50090-7501-0A-S Medication Solutions27 January 2025
3 syringe, plastic in 1 carton / 3 mL in 1 syringe, plastic50090-8145-0A-S Medication Solutions8 October 2026
2 syringe, plastic in 1 carton / 3 mL in 1 syringe, plastic72603-745-02NorthStar Rx1 March 2026
3 syringe, plastic in 1 carton / 3 mL in 1 syringe, plastic72603-745-03NorthStar Rx1 March 2026

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 25 January 2010Drugs@FDA
EU (EMA)AuthorisedEMA medicines data
India (CDSCO)Not yet confirmed against CDSCO approval lists—
AustriaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
BelgiumRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
BulgariaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
CroatiaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
CyprusRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
CzechiaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
DenmarkRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
EstoniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
FinlandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
FranceRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
GermanyRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
GreeceRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
HungaryRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
IcelandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
IrelandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
ItalyRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LatviaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LiechtensteinRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LithuaniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LuxembourgRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
MaltaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
NetherlandsRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
NorwayRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
PolandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
PortugalRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
RomaniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SlovakiaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SloveniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SpainRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SwedenRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
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 Liraglutide 18 mg/3 mL injection.

Compare all 2

Clinical summary

Liraglutide is a GLP-1 receptor agonist indicated as an adjunct to diet and exercise to improve glycemic control in adults and pediatric patients aged 10 years and older with type 2 diabetes mellitus, among other approved uses. MedsAcross supplies Liraglutide 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 Liraglutide

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

Data sources

Need Liraglutide 18 mg/3 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.