Medicine
Fenoprofen 300 mg capsule
Fenoprofen 300 mg capsule is a generic prescription medicine for oral use, made by 3 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
Export supply from India to licensed buyers
Typical lead time
On request
Counted from payment and complete documents
Shipping
Ambient
Store at room temperature 20°C to 25°C (68°F to 77°F), excursions permitted…
Key facts
- Active ingredient (INN)
- Fenoprofen
- Brand
- Sold under the generic name
- Strength
- 300 mg
- Dosage form
- Capsule
- Route
- Oral
- Packs
- 100 capsules
- Manufacturers
- Coral Way PharmaMisemer PharmaceuticalsRising Pharma Holdings
- Origin register
- US FDA, United States
- Storage
- Store at room temperature 20°C to 25°C (68°F to 77°F), excursions permitted between 15°C to 30°C (59°F to 86°F).
- Cold chain
- Not required on record
- Prescription status
- Prescription only
- Controlled substance
- Not recorded as controlled
- ATC code
- M01AE04 Fenoprofen
- HS code (indicative)
- 3004.90Indicative only. Your customs broker confirms the final tariff code.
- Marketing category
- marketed
- Marketed since
- 1 November 2023
- Identifiers
- RxCUI 197694, 197695, 858116DailyMed set ID d33ad329-1ca6-ac2e-e053-2995a90a15c5, 56b07659-1fd8-4c3e-e063-6294a90a8908, 4aa38cca-9f8f-4ab6-8103-4f1f48801a43NDC 0276-0502, 85437-502, 16571-887Application ANDA215548, ANDA214475
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.
| Pack | Code | Labeler | Marketed since |
|---|---|---|---|
| 100 capsule in 1 bottle | 85437-502-10 | Coral Way Pharma | 15 July 2026 |
| 100 capsule in 1 bottle | 0276-0502-10 | Misemer Pharmaceuticals | 1 November 2023 |
| 100 capsule in 1 bottle | 16571-887-01 | Rising Pharma Holdings | 26 July 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.
| Register | Status | Source |
|---|---|---|
| US FDA | Listed, marketed | Source record for this pageChecked 12 November 2026 |
| US FDA | First approved 16 March 1976 | 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 Fenoprofen 300 mg capsule.
Other strengths and forms of Fenoprofen
Clinical summary
Fenoprofen is a nonsteroidal anti-inflammatory drug indicated for relief of mild to moderate pain in adults, among other approved uses. It is available as capsules for oral use. MedsAcross supplies Fenoprofen 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 FenoprofenFor healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.
Data sources
- DailyMed label record · Checked 12 November 2026
- Fenoprofen Calcium prescribing information (Misemer Pharmaceuticals) · U.S. National Library of Medicine, DailyMed
Need Fenoprofen 300 mg capsule 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.