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MedsAcross

Medicine

Terbutaline 1 mg/1 mL injection

Terbutaline · Subcutaneous
Available on requestPrescription onlyUS FDAGeneric name

Terbutaline 1 mg/1 mL injection is a generic prescription medicine for subcutaneous use, made by 4 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.

Availability

Available on request

Export supply from India to licensed buyers

Typical lead time

On request

Counted from payment and complete documents

Shipping

Ambient

Store at 20° to 25°C (68° to 77°F). Protect from light by storing vials in…

Key facts

Active ingredient (INN)
Terbutaline
Brand
Sold under the generic name
Strength
1 mg/1 mL
Dosage form
Injection
Route
Subcutaneous
Packs
10 vials of 1 mL, 25 vials of 1 mL, 1 vial of 1 mL and 2 more
Manufacturers
Hikma PharmaceuticalsFresenius KabiHenry ScheinMedical Purchasing Solutions
Origin register
US FDA, United States
Storage
Store at 20° to 25°C (68° to 77°F). Protect from light by storing vials in original carton until dispensed.
Cold chain
Not required on record
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
R03AC03 Terbutaline
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
20 May 2009
Identifiers
RxCUI 857635DailyMed set ID 0f4d3249-e022-40b6-b93d-f605e8522207, 613df3cb-4d55-4d12-ab08-a932481aaa0b, 9f4b177e-4d7d-4255-afeb-522c7d4594c6 +2NDC 0143-9375, 0143-9746, 0404-9962 +2Application ANDA078630, ANDA076887

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
10 vial in 1 carton / 1 mL in 1 vial0143-9375-10Hikma Pharmaceuticals20 May 2009
10 vial in 1 carton / 1 mL in 1 vial0143-9746-10Hikma Pharmaceuticals20 May 2009
25 vial, single-use in 1 tray / 1 mL in 1 vial, single-use63323-665-01Fresenius Kabi10 March 2011
1 vial in 1 bag / 1 mL in 1 vial0404-9962-01Henry Schein12 January 2022
1 vial in 1 bag / 1 mL in 1 vial71872-7080-1Medical Purchasing Solutions6 March 2018

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 25 March 1974Drugs@FDA
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 Terbutaline

Clinical summary

Terbutaline is a prescription medicine indicated for the prevention and reversal of bronchospasm in patients 12 years of age and older with asthma and reversible bronchospasm associated with bronchitis and emphysema. MedsAcross supplies Terbutaline 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 Terbutaline

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

Data sources

Need Terbutaline 1 mg/1 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.