Medicine
Phesgo 30000 units/1200 mg/600 mg per 15 mL injection
Phesgo 30000 units/1200 mg/600 mg per 15 mL injection is a prescription medicine containing Hyaluronidase (human recombinant), Pertuzumab and Trastuzumab for subcutaneous use, marketed by Genentech, 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
Export supply from India to licensed buyers
Typical lead time
On request
Counted from payment and complete documents
Shipping
Cold chain
Store PHESGO vials in the refrigerator at 2°C to 8°C (36°F to 46°F) in the…
Key facts
- Active ingredient (INN)
- Hyaluronidase (human recombinant), Pertuzumab and Trastuzumab
- Brand
- Phesgo
- Strength
- 30000 units/1200 mg/600 mg per 15 mL
- Dosage form
- Injection
- Route
- Subcutaneous
- Packs
- 1 vial
- Marketing authorisation holder
- Genentech
- Manufacturer
- Genentech
- Origin register
- US FDA, United States
- Storage
- Store PHESGO vials in the refrigerator at 2°C to 8°C (36°F to 46°F) in the original carton to protect from light. Do not freeze. Do not shake.
- Cold chain
- Yes, shipped temperature controlled
- Prescription status
- Prescription only
- Controlled substance
- Not recorded as controlled
- HS code (indicative)
- 3002.15Indicative only. Your customs broker confirms the final tariff code.
- Marketing category
- marketed
- Marketed since
- 29 June 2020
- Identifiers
- RxCUI 2382604, 2382609, 2383305 +1DailyMed set ID 27dd5e6b-72cd-458d-a015-cf4dab5800daNDC 50242-245Application BLA761170
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
| Pack | Code | Labeler | Marketed since |
|---|---|---|---|
| 1 vial, single-dose in 1 carton / 15 mL in 1 vial, single-dose | 50242-245-01 | Genentech | 29 June 2020 |
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.
| Register | Status | Source |
|---|---|---|
| US FDA | Listed, marketed | Source record for this pageChecked 12 November 2026 |
| EU (EMA) | Not recorded | — |
| India (CDSCO) | Not yet confirmed against CDSCO approval lists | — |
| United States | Registered | US 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
Other strengths and forms of Hyaluronidase (human recombinant), Pertuzumab and Trastuzumab
Clinical summary
Hyaluronidase (human recombinant), Pertuzumab and Trastuzumab is a fixed-dose combination of an HER2/neu receptor antagonist and an endoglycosidase indicated for use in combination with chemotherapy as, among other approved uses. MedsAcross supplies Hyaluronidase (human recombinant), Pertuzumab and Trastuzumab 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 Hyaluronidase (human recombinant), Pertuzumab and TrastuzumabFor healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.
Data sources
- DailyMed label record · Checked 12 November 2026
- Phesgo prescribing information (Genentech) · U.S. National Library of Medicine, DailyMed
Need Phesgo 30000 units/1200 mg/600 mg per 15 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.