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Medicine

Eptifibatide 75 mg/100 mL injection

Eptifibatide · Intravenous
Available on requestPrescription onlyUS FDA Cold chainGeneric name

Eptifibatide 75 mg/100 mL injection is a generic prescription medicine for intravenous use, made by 8 labelers, 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 at 25°C (77°F), excursions permitted to 15° to 30°C (59° to 86°F).

Key facts

Active ingredient (INN)
Eptifibatide
Brand
Sold under the generic name
Strength
75 mg/100 mL
Dosage form
Injection
Route
Intravenous
Packs
1 vial of 100 mL, 100 mL and 7 more
Manufacturers
EugiaIndiaMylan InstitutionalSlate Run PharmaceuticalsAvenacyBaxter HealthcareHainan Shuangcheng PharmaceuticalsMeitheal PharmaceuticalsSagent Pharmaceuticals
Origin register
US FDA, United States
Storage
Store at 25°C (77°F), excursions permitted to 15° to 30°C (59° to 86°F).
Cold chain
Yes, shipped temperature controlled
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
B01AC16 Eptifibatide
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
8 December 2015
Identifiers
RxCUI 200349, 1736470, 1736477DailyMed set ID a7a89c59-22fb-41fd-b70a-ac2395717db1, 88a37f9c-496b-4a6b-9665-4550abba04f1, 3e7e7cd3-8efa-4d91-a5ab-7fd78b0cc65e +7NDC 72078-026, 67457-631, 71288-413 +7Application ANDA203258, ANDA213599, ANDA209864 +4

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

Packs from every labeler of this generic presentation.

PackCodeLabelerMarketed since
1 vial, single-dose in 1 carton / 100 mL in 1 vial, single-dose55150-218-99EugiaIndia8 December 2015
1 vial in 1 carton / 100 mL in 1 vial67457-631-10Mylan Institutional13 December 2018
1 vial in 1 carton / 100 mL in 1 vial72078-026-10Mylan Institutional20 November 2020
100 mL in 1 vial70436-027-80Slate Run Pharmaceuticals22 July 2019
100 mL in 1 vial70436-163-80Slate Run Pharmaceuticals1 December 2020
1 vial, single-dose in 1 carton / 100 mL in 1 vial, single-dose0338-9558-10Baxter Healthcare1 February 2019
1 vial, single-dose in 1 carton / 100 mL in 1 vial, single-dose52958-040-01Hainan Shuangcheng Pharmaceuticals21 April 2022
1 vial, single-dose in 1 carton / 100 mL in 1 vial, single-dose71288-413-51Meitheal Pharmaceuticals9 May 2024
1 vial in 1 carton / 100 mL in 1 vial25021-408-51Sagent Pharmaceuticals15 July 2018
1 vial, single-dose in 1 carton / 100 mL in 1 vial, single-dose83634-301-51Avenacy31 January 2024

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 18 May 1998Drugs@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

Other strengths and forms of Eptifibatide

Clinical summary

Eptifibatide is a platelet aggregation inhibitor indicated for treatment of acute coronary syndrome (ACS) managed medically or with percutaneous coronary intervention (PCI), among other approved uses. It is available as injection for intravenous use. MedsAcross supplies Eptifibatide 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 Eptifibatide

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

Data sources

Need Eptifibatide 75 mg/100 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.