Medicine
Augmentin 125 mg/31.25 mg per 5 mL powder for oral suspension
Augmentin 125 mg/31.25 mg per 5 mL powder for oral suspension is a prescription medicine containing Amoxicillin and Clavulanate for oral use, marketed by Allegis Holdings, 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
Store dry powder at or below 25°C (77°F). Store reconstituted suspension under…
Key facts
- Active ingredient (INN)
- Amoxicillin and Clavulanate
- Brand
- Augmentin
- Strength
- 125 mg/31.25 mg per 5 mL
- Dosage form
- Powder for oral suspension
- Route
- Oral
- Packs
- 75 mL, 100 mL, 150 mL
- Marketing authorisation holder
- Allegis Holdings
- Manufacturer
- Allegis Holdings
- Origin register
- US FDA, United States
- Storage
- Store dry powder at or below 25°C (77°F). Store reconstituted suspension under refrigeration.
- Cold chain
- Not required on record
- Prescription status
- Prescription only
- Controlled substance
- Not recorded as controlled
- HS code (indicative)
- 3004.10Indicative only. Your customs broker confirms the final tariff code.
- Marketing category
- marketed
- Marketed since
- 1 September 2023
- Identifiers
- RxCUI 617302, 617333DailyMed set ID 04a31a42-d79e-bbb4-e063-6394a90a63eeNDC 71297-240Application NDA050575
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 |
|---|---|---|---|
| 75 mL in 1 bottle | 71297-240-34 | Allegis Holdings | 20 February 2024 |
| 100 mL in 1 bottle | 71297-240-35 | Allegis Holdings | 1 September 2023 |
| 150 mL in 1 bottle | 71297-240-36 | Allegis Holdings | 1 September 2023 |
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 6 August 1984 | 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 Amoxicillin and Clavulanate 125 mg/31.25 mg per 5 mL powder for oral suspension.
Other strengths and forms of Amoxicillin and Clavulanate
Clinical summary
Amoxicillin and Clavulanate is a fixed-dose combination of a penicillin-class antibacterial and a beta lactamase inhibitor indicated for the treatment of infections in adults and pediatric patients, among other approved uses. MedsAcross supplies Amoxicillin and Clavulanate 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 Amoxicillin and ClavulanateFor healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.
Data sources
- DailyMed label record · Checked 12 November 2026
- Augmentin prescribing information (Allegis Holdings) · U.S. National Library of Medicine, DailyMed
Need Augmentin 125 mg/31.25 mg per 5 mL powder for oral 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.