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Medicine

TISSEEL Fibrin Sealant kit

Fibrinogen human · Baxter Healthcare
Available on requestPrescription onlyUS FDA

TISSEEL Fibrin Sealant kit is a prescription medicine containing Fibrinogen human, marketed by Baxter Healthcare, 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.

Availability

Available on request

Export supply from India to licensed buyers

Typical lead time

On request

Counted from payment and complete documents

Shipping

Ambient

Storage as on the product label

Key facts

Active ingredient (INN)
Fibrinogen human
Brand
TISSEEL Fibrin Sealant
Dosage form
Kit
Packs
1 kit and 3 more
Marketing authorisation holder
Baxter Healthcare
Manufacturer
Baxter Healthcare
Origin register
US FDA, United States
Cold chain
Not required on record
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
B02BB01 Fibrinogen
HS code (indicative)
3002.12Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
1 May 1998
Identifiers
NDC 0338-4210, 0338-4301, 0338-4303 +3Application BLA103980

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, glass * 1 mL in 1 vial, glass * 1 mL in 1 vial, glass * 1 mL in 1 vial, glass0338-4210-02Baxter Healthcare1 May 1998
1 kit in 1 carton * 2 mL in 1 vial, glass * 2 mL in 1 vial, glass * 2 mL in 1 vial, glass * 2 mL in 1 vial, glass0338-4211-04Baxter Healthcare1 May 1998
1 kit in 1 carton * 5 mL in 1 vial, glass * 5 mL in 1 vial, glass * 5 mL in 1 vial, glass * 5 mL in 1 vial, glass0338-4212-10Baxter Healthcare1 May 1998
1 kit in 1 carton * 1 mL in 1 vial, glass * 1 mL in 1 vial, glass * 1 mL in 1 vial, glass * 1 mL in 1 vial, glass0338-4301-02Baxter Healthcare1 May 1998
1 kit in 1 carton * 2 mL in 1 vial, glass * 2 mL in 1 vial, glass * 2 mL in 1 vial, glass * 2 mL in 1 vial, glass0338-4302-04Baxter Healthcare1 May 1998
1 kit in 1 carton * 5 mL in 1 vial, glass * 5 mL in 1 vial, glass * 5 mL in 1 vial, glass * 5 mL in 1 vial, glass0338-4303-10Baxter Healthcare1 May 1998

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

Other strengths and forms of Fibrinogen human

Clinical summary

Fibrinogen human is a human blood coagulation factor indicated for the treatment of acute bleeding episodes in pediatric and adult patients with congenital fibrinogen deficiency, including afibrinogenemia and hypofibrinogenemia, among other approved uses. MedsAcross supplies Fibrinogen human 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 Fibrinogen human

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

Data sources

Need TISSEEL Fibrin Sealant 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.