Medicine
Kenalog-40 400 mg/10 mL injectable suspension
Kenalog-40 400 mg/10 mL injectable suspension is a prescription medicine containing Triamcinolone acetonide for intra-articular, intramuscular use, marketed by ER Squibb & Sons, 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
Export supply from India to licensed buyers
Typical lead time
On request
Counted from payment and complete documents
Shipping
Ambient
Do not refrigerate. Store at controlled room temperature, 20°C to 25°C (68°F…
Key facts
- Active ingredient (INN)
- Triamcinolone acetonide
- Brand
- Kenalog-40
- Strength
- 400 mg/10 mL
- Dosage form
- Injectable suspension
- Route
- Intra-articular, intramuscular
- Packs
- 1 vial of 10 mL
- Marketing authorisation holder
- ER Squibb & Sons
- Manufacturers
- ER Squibb & SonsA-S Medication Solutions
- Origin register
- US FDA, United States
- Storage
- Do not refrigerate. Store at controlled room temperature, 20°C to 25°C (68°F to 77°F), protect from temperatures below 20°C (68°F). Excursions are permitted between 15°C and 30°C (59°F and 86°F). Once in use: Chemical and physical in-use stability has been demonstrated for 28 days below 25°C (77°F).
- Cold chain
- Not required on record
- Prescription status
- Prescription only
- Controlled substance
- Not recorded as controlled
- HS code (indicative)
- 3004.32Indicative only. Your customs broker confirms the final tariff code.
- Marketing category
- marketed
- Marketed since
- 1 June 2009
- Identifiers
- RxCUI 1085754, 1085756, 1792144 +5DailyMed set ID cf970688-cd77-b95c-4bd9-c541590e9722, 4ce116aa-b330-4da9-9cdd-ba8e6be0c4adNDC 0003-0293, 50090-0819Application NDA014901
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, multi-dose in 1 carton / 10 mL in 1 vial, multi-dose | 0003-0293-28 | ER Squibb & Sons | 1 June 2009 |
| 1 vial, multi-dose in 1 carton / 10 mL in 1 vial, multi-dose | 50090-0819-0 | A-S Medication Solutions | 28 November 2014 |
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 |
| US FDA | First approved 23 October 1958 | Drugs@FDA |
| 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
Alternatives
Other makers and brands of Triamcinolone acetonide 400 mg/10 mL injectable suspension.
Other strengths and forms of Triamcinolone acetonide
Clinical summary
Triamcinolone acetonide is a corticosteroid indicated as adjunctive therapy for short-term administration (to tide the patient over an acute episode or exacerbation) in acute gouty arthritis, acute and subacute bursitis, acute nonspecific tenosynovitis, epicondylitis, rheumatoid arthritis. MedsAcross supplies Triamcinolone acetonide 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 Triamcinolone acetonideFor healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.
Data sources
- DailyMed label record · Checked 12 November 2026
- KENALOG-10 prescribing information (ER Squibb & Sons) · U.S. National Library of Medicine, DailyMed
Need Kenalog-40 400 mg/10 mL injectable suspension 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.