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MedsAcross

Medicine

Genotropin kit

Somatropin · Pfizer Laboratories
Available on requestPrescription onlyUS FDA Cold chain

Genotropin kit is a prescription medicine containing Somatropin, marketed by Pfizer Laboratories, 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 GENOTROPIN lyophilized powder under refrigeration at 36°F to 46°F (2°C…

Key facts

Active ingredient (INN)
Somatropin
Brand
Genotropin
Dosage form
Kit
Packs
1 cartridge, 7 cartridges and 9 more
Marketing authorisation holder
Pfizer Laboratories
Manufacturer
Pfizer Laboratories
Origin register
US FDA, United States
Storage
Store GENOTROPIN lyophilized powder under refrigeration at 36°F to 46°F (2°C to 8°C) until the expiration date. Store under refrigeration at 36°F to 46°F (2°C to 8°C) between each use, for up to 28 days.
Cold chain
Yes, shipped temperature controlled
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
H01AC01 Somatropin
HS code (indicative)
3002.15Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
20 December 1995
Identifiers
RxCUI 241975, 762830, 762833 +7DailyMed set ID ffebf88b-d257-4542-9808-74d9b7167765NDC 0013-2650, 0013-2646, 0013-2651 +9Application BLA020280

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 cartridge in 1 carton / 1 kit in 1 cartridge0013-2626-81Pfizer Laboratories20 December 1995
1 cartridge in 1 carton / 1 kit in 1 cartridge0013-2646-81Pfizer Laboratories20 December 1995
7 cartridge in 1 carton / 1 kit in 1 cartridge0013-2649-02Pfizer Laboratories20 December 1995
7 cartridge in 1 carton / 1 kit in 1 cartridge0013-2650-02Pfizer Laboratories20 December 1995
7 cartridge in 1 carton / 1 kit in 1 cartridge0013-2651-02Pfizer Laboratories20 December 1995
7 cartridge in 1 carton / 1 kit in 1 cartridge0013-2652-02Pfizer Laboratories20 December 1995
7 cartridge in 1 carton / 1 kit in 1 cartridge0013-2653-02Pfizer Laboratories20 December 1995
7 cartridge in 1 carton / 1 kit in 1 cartridge0013-2654-02Pfizer Laboratories20 December 1995
7 cartridge in 1 carton / 1 kit in 1 cartridge0013-2655-02Pfizer Laboratories20 December 1995
7 cartridge in 1 carton / 1 kit in 1 cartridge0013-2656-02Pfizer Laboratories20 December 1995
7 cartridge in 1 carton / 1 kit in 1 cartridge0013-2657-02Pfizer Laboratories20 December 1995
7 cartridge in 1 carton / 1 kit in 1 cartridge0013-2658-02Pfizer Laboratories20 December 1995

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 16 October 1986Drugs@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 Somatropin kit.

Compare all 5

Other strengths and forms of Somatropin

Clinical summary

Somatropin is a recombinant human growth hormone indicated for pediatric Patients, among other approved uses. It is available as kits and injection for subcutaneous and intramuscular use. MedsAcross supplies Somatropin 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 Somatropin

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

Data sources

Need Genotropin 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.