Medicine
Naproxen 375 mg delayed-release tablet
Naproxen 375 mg delayed-release tablet is a generic prescription medicine for oral use, made by 6 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 20° to 25°C (68° to 77°F),.
Key facts
- Active ingredient (INN)
- Naproxen
- Brand
- Sold under the generic name
- Strength
- 375 mg
- Dosage form
- Delayed-release tablet
- Route
- Oral
- Packs
- 100 tablets, 500 tablets, 14 tablets and 11 more
- Manufacturers
- Aurobindo PharmaIndiaCiplaIndiaProficient RxANI PharmaceuticalsSunrise PharmaceuticalTruPharma
- Origin register
- US FDA, United States
- Storage
- Store at 20° to 25°C (68° to 77°F),.
- Cold chain
- Not required on record
- Prescription status
- Prescription only
- Controlled substance
- Not recorded as controlled
- ATC code
- G02CC02 Naproxen
- HS code (indicative)
- 3004.90Indicative only. Your customs broker confirms the final tariff code.
- Marketing category
- marketed
- Marketed since
- 5 July 2016
- Identifiers
- RxCUI 311915, 603103DailyMed set ID 004bb832-29d5-add0-e063-6394a90a90f4, 67815abd-5e97-4ccb-ac9b-28c2ef6123e7, 052e6fe3-d619-42c3-b64e-67c7aaf7271c +3NDC 52817-380, 59651-986, 70954-925 +3Application ANDA216908, ANDA075390, ANDA218497 +1
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 tablet, delayed release in 1 bottle | 59651-986-01 | Aurobindo PharmaIndia | 8 May 2025 |
| 500 tablet, delayed release in 1 bottle | 59651-986-05 | Aurobindo PharmaIndia | 8 May 2025 |
| 100 tablet, delayed release in 1 bottle | 69097-851-07 | CiplaIndia | 5 July 2016 |
| 100 tablet, delayed release in 1 bottle | 70954-925-10 | ANI Pharmaceuticals | 13 June 2024 |
| 100 tablet, delayed release in 1 bottle, plastic | 11534-211-01 | Sunrise Pharmaceutical | 9 December 2025 |
| 100 tablet, delayed release in 1 bottle, plastic | 52817-380-10 | TruPharma | 1 August 2023 |
| 14 tablet, delayed release in 1 bottle | 71205-060-14 | Proficient Rx | 1 June 2018 |
| 15 tablet, delayed release in 1 bottle | 71205-060-15 | Proficient Rx | 1 June 2018 |
| 20 tablet, delayed release in 1 bottle | 71205-060-20 | Proficient Rx | 1 June 2018 |
| 30 tablet, delayed release in 1 bottle | 71205-060-30 | Proficient Rx | 1 June 2018 |
| 40 tablet, delayed release in 1 bottle | 71205-060-40 | Proficient Rx | 1 June 2018 |
| 45 tablet, delayed release in 1 bottle | 71205-060-45 | Proficient Rx | 1 June 2018 |
| 60 tablet, delayed release in 1 bottle | 71205-060-60 | Proficient Rx | 1 June 2018 |
| 90 tablet, delayed release in 1 bottle | 71205-060-90 | Proficient Rx | 1 June 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.
| Register | Status | Source |
|---|---|---|
| US FDA | Listed, marketed | Source record for this pageChecked 12 November 2026 |
| US FDA | First approved 11 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
Other strengths and forms of Naproxen
Clinical summary
Naproxen is a nonsteroidal anti-inflammatory drug indicated for the relief of the signs and symptoms of. It is available as tablets, delayed-release tablets and extended-release tablets for oral use. MedsAcross supplies Naproxen 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 NaproxenFor healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.
Data sources
- DailyMed label record · Checked 12 November 2026
- Naproxen prescribing information (Acella Pharmaceuticals) · U.S. National Library of Medicine, DailyMed
Need Naproxen 375 mg delayed-release tablet 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.