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MedsAcross

Medicine

Somavert kit

Pegvisomant · Pharmacia & Upjohn
Available on requestPrescription onlyUS FDA Cold chain

Somavert kit is a prescription medicine containing Pegvisomant, marketed by Pharmacia & Upjohn, 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

Do not freeze. If not used within 30 days at room temperature, the vial(s)…

Key facts

Active ingredient (INN)
Pegvisomant
Brand
Somavert
Dosage form
Kit
Packs
1 kit, 30 kits and 7 more
Marketing authorisation holder
Pharmacia & Upjohn
Manufacturer
Pharmacia & Upjohn
Origin register
US FDA, United States
Storage
Do not freeze. If not used within 30 days at room temperature, the vial(s) should be discarded. The prefilled syringe(s) may be stored at a temperature up to 30°C (86°F) until the expiration date printed on the carton, at which point they should be discarded. Prior to reconstitution: • The One Day Package of SOMAVERT should be stored in a refrigerator at 2°C to 8°C (36°F to 46°F).
Cold chain
Yes, shipped temperature controlled
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
H01AX01 Pegvisomant
HS code (indicative)
3002.15Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
1 October 2016
Identifiers
RxCUI 403806, 403807, 403808 +7DailyMed set ID 3cbb485b-6df1-49ce-8747-592b395b1988NDC 0009-7200, 0009-7199, 0009-7166 +2Application BLA021106

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

PackCodeLabelerMarketed since
1 kit in 1 carton * 1 mL in 1 vial, single-dose * 1 mL in 1 syringe0009-7166-01Pharmacia & Upjohn1 October 2016
30 kit in 1 carton / 1 kit in 1 kit * 1 mL in 1 vial, single-dose * 1 mL in 1 syringe0009-7166-30Pharmacia & Upjohn17 January 2022
1 kit in 1 carton * 1 mL in 1 vial, single-dose * 1 mL in 1 syringe0009-7168-01Pharmacia & Upjohn1 October 2016
30 kit in 1 carton / 1 kit in 1 kit * 1 mL in 1 vial, single-dose * 1 mL in 1 syringe0009-7168-30Pharmacia & Upjohn17 January 2022
1 kit in 1 carton * 1 mL in 1 vial, single-dose * 1 mL in 1 syringe0009-7188-01Pharmacia & Upjohn1 October 2016
30 kit in 1 carton / 1 kit in 1 kit * 1 mL in 1 vial, single-dose * 1 mL in 1 syringe0009-7188-30Pharmacia & Upjohn17 January 2022
1 kit in 1 carton * 1 mL in 1 syringe * 1 mL in 1 vial, single-dose0009-7199-01Pharmacia & Upjohn1 October 2016
30 kit in 1 carton / 1 kit in 1 kit * 1 mL in 1 syringe * 1 mL in 1 vial, single-dose0009-7199-30Pharmacia & Upjohn17 January 2022
1 kit in 1 carton * 1 mL in 1 vial, single-dose * 1 mL in 1 syringe0009-7200-01Pharmacia & Upjohn1 October 2016
30 kit in 1 carton / 1 kit in 1 kit * 1 mL in 1 vial, single-dose * 1 mL in 1 syringe0009-7200-30Pharmacia & Upjohn17 January 2022

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 March 2003Drugs@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

Clinical summary

Pegvisomant is a prescription medicine indicated for the treatment of acromegaly in patients who have had an inadequate response to surgery or radiation therapy, or for whom these therapies are not appropriate. It is available as kits. MedsAcross supplies Pegvisomant 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 Pegvisomant

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

Data sources

Need Somavert kit 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.