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Medicine

Panzyga 20000 mg/200 mL injection

Human immunoglobulin g · Intravenous · Octapharma
Available on requestPrescription onlyUS FDA Cold chain

Panzyga 20000 mg/200 mL injection is a prescription medicine containing Human immunoglobulin g for intravenous use, marketed by Octapharma, 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. Store PANZYGA for 36 months at +2°C to +8°C (36°F to 46°F) from…

Key facts

Active ingredient (INN)
Human immunoglobulin g
Brand
Panzyga
Strength
20000 mg/200 mL
Dosage form
Injection
Route
Intravenous
Packs
1 bottle of 200 mL
Marketing authorisation holder
Octapharma
Manufacturers
OctapharmaPfizer Laboratories
Origin register
US FDA, United States
Storage
Do not freeze. Store PANZYGA for 36 months at +2°C to +8°C (36°F to 46°F) from the date of manufacture. Within its shelf-life, the product may be stored at ≤ +25°C (77°F) for up to 12 months. After storage at ≤ +25°C (77°F), either use immediately or discard the product.
Cold chain
Yes, shipped temperature controlled
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
J06BA02 Human immunoglobulin g
HS code (indicative)
3002.12Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
12 November 2018
Identifiers
RxCUI 2102435, 2102440, 2102455 +7DailyMed set ID e2cc5ddf-119e-ade3-79c2-c712cfbee099, 9306c5f7-ddf9-5190-d0c1-31ba9ca2d0e0NDC 0069-1415, 68982-822Application BLA125587

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 bottle, glass in 1 carton / 200 mL in 1 bottle, glass68982-822-05Octapharma12 November 2018
1 bottle, glass in 1 carton / 200 mL in 1 bottle, glass0069-1415-02Pfizer Laboratories9 August 2019

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
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 Human immunoglobulin g 20000 mg/200 mL injection.

Compare all 3

Other strengths and forms of Human immunoglobulin g

Clinical summary

Human immunoglobulin g is a human immunoglobulin G indicated for the treatment of adults and pediatric patients 2 years of age and older with primary humoral immunodeficiency (PI). MedsAcross supplies Human immunoglobulin g 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 Human immunoglobulin g

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

Data sources

Need Panzyga 20000 mg/200 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.