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Medicine

Auvi-Q 0.15 mg/0.15 mL injection

Epinephrine · Intramuscular · kaleo
Available on requestPrescription onlyUS FDA

Auvi-Q 0.15 mg/0.15 mL injection is a prescription medicine containing Epinephrine for intramuscular use, marketed by kaleo, 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

Do not freeze. Store at 20°C to 25°C (68°F to 77°F), excursions permitted to…

Key facts

Active ingredient (INN)
Epinephrine
Brand
Auvi-Q
Strength
0.15 mg/0.15 mL
Dosage form
Injection
Route
Intramuscular
Packs
2 dose packs, 1 dose pack and 7 more
Marketing authorisation holder
kaleo
Manufacturers
kaleoMedical Purchasing SolutionsSportpharm
Origin register
US FDA, United States
Storage
Do not freeze. Store at 20°C to 25°C (68°F to 77°F), excursions permitted to 15°C to 30°C (59°F to 86°F). Protect from light. Epinephrine is light sensitive and should be stored in the outer case.
Cold chain
Not required on record
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
A01AD01 Epinephrine
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
15 November 2012
Identifiers
RxCUI 1305268, 1305269, 1870205 +3DailyMed set ID 5f40988b-8365-4f7b-84d1-b88e053725cf, 6180fb40-7fca-4602-b3da-ce62b8cd2470, 296a9023-b5c6-6102-e063-6294a90af87e +3NDC 85766-277, 60842-021, 85766-276 +7Application NDA201739

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
2 dose pack in 1 carton / .1 mL in 1 dose pack60842-021-02kaleo5 September 2024
2 dose pack in 1 carton / .15 mL in 1 dose pack60842-022-02kaleo5 November 2024
2 dose pack in 1 carton / .3 mL in 1 dose pack60842-023-02kaleo10 September 2024
1 dose pack in 1 bag / .15 mL in 1 dose pack71872-7172-1Medical Purchasing Solutions15 July 2019
1 dose pack in 1 bag / .3 mL in 1 dose pack71872-7173-1Medical Purchasing Solutions15 July 2019
1 dose pack in 1 bag / .3 mL in 1 dose pack71872-7329-1Medical Purchasing Solutions25 October 2024
1 dose pack in 1 bag / .15 mL in 1 dose pack71872-7333-1Medical Purchasing Solutions15 November 2024
2 dose pack in 1 carton / .1 mL in 1 dose pack85766-275-02Sportpharm18 September 2026
2 dose pack in 1 carton / .15 mL in 1 dose pack85766-276-02Sportpharm18 September 2026
2 dose pack in 1 carton / .3 mL in 1 dose pack85766-277-02Sportpharm18 September 2026

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 8 June 1951Drugs@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 Epinephrine 0.15 mg/0.15 mL injection.

Compare 1

Other strengths and forms of Epinephrine

Clinical summary

Epinephrine is a catecholamine. It is available as injection, nasal spray and kits for intramuscular, subcutaneous and intravenous use. MedsAcross supplies Epinephrine 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 Epinephrine

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

Data sources

Need Auvi-Q 0.15 mg/0.15 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.