Medicine
Morphine 15 mg extended-release tablet
Morphine 15 mg extended-release tablet is a generic prescription medicine for oral use, made by 7 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 25°C (77°F), excursions permitted between 15° to 30°C (59° to 86°F)…
Key facts
- Active ingredient (INN)
- Morphine
- Brand
- Sold under the generic name
- Strength
- 15 mg
- Dosage form
- Extended-release tablet
- Route
- Oral
- Packs
- 100 tablets, 10 tablets, 500 tablets and 32 more
- Manufacturers
- Sun Pharmaceutical IndustriesIndiaLupinIndiaBryant Ranch PrepackSpecGxAmerican Health PackagingMajor PharmaceuticalsRhodes Pharmaceuticals
- Origin register
- US FDA, United States
- Storage
- Store at 25°C (77°F), excursions permitted between 15° to 30°C (59° to 86°F). Store morphine sulfate extended-release tablets securely and dispose of properly.
- Cold chain
- Not required on record
- Prescription status
- Prescription only
- Controlled substance
- Schedule CII
- ATC code
- N02AA01 Morphine
- HS code (indicative)
- 3004.90Indicative only. Your customs broker confirms the final tariff code.
- Marketing category
- marketed
- Marketed since
- 31 July 2003
- Identifiers
- RxCUI 891881, 891888, 891874 +2DailyMed set ID f915420d-981d-455b-b4cf-67c8e201a136, 73a39ce5-b2ab-47b9-8860-796f1d5bc8d8, dbb37dfd-0196-45f7-b9ca-393f56cf1d28 +7NDC 68084-157, 71335-0736, 0904-6557 +7Application ANDA074862, ANDA078761, ANDA203602 +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, film coated, extended release in 1 bottle | 43386-540-01 | LupinIndia | 16 December 2015 |
| 100 tablet, film coated, extended release in 1 bottle | 63304-450-01 | Sun Pharmaceutical IndustriesIndia | 11 May 2012 |
| 10 tablet, film coated, extended release in 1 bottle | 63304-450-03 | Sun Pharmaceutical IndustriesIndia | 11 May 2012 |
| 500 tablet, film coated, extended release in 1 bottle | 63304-450-05 | Sun Pharmaceutical IndustriesIndia | 11 May 2012 |
| 100 tablet, film coated, extended release in 1 bottle, plastic | 42858-801-01 | Rhodes Pharmaceuticals | 14 January 2011 |
| 100 tablet, extended release in 1 bottle | 0406-8315-01 | SpecGx | 31 July 2003 |
| 1 tablet, extended release in 1 blister pack | 0406-8315-23 | SpecGx | 31 July 2003 |
| 100 tablet, extended release in 1 blister pack | 0406-8315-62 | SpecGx | 31 July 2003 |
| 100 tablet, film coated, extended release in 1 bottle | 63629-1087-1 | Bryant Ranch Prepack | 11 May 2012 |
| 26 tablet, film coated, extended release in 1 bottle | 63629-4483-0 | Bryant Ranch Prepack | 3 January 2022 |
| 30 tablet, film coated, extended release in 1 bottle | 63629-4483-1 | Bryant Ranch Prepack | 20 April 2011 |
| 60 tablet, film coated, extended release in 1 bottle | 63629-4483-2 | Bryant Ranch Prepack | 14 April 2011 |
| 90 tablet, film coated, extended release in 1 bottle | 63629-4483-3 | Bryant Ranch Prepack | 11 July 2011 |
| 120 tablet, film coated, extended release in 1 bottle | 63629-4483-4 | Bryant Ranch Prepack | 3 January 2022 |
| 40 tablet, film coated, extended release in 1 bottle | 63629-4483-5 | Bryant Ranch Prepack | 3 January 2022 |
| 14 tablet, film coated, extended release in 1 bottle | 63629-4483-6 | Bryant Ranch Prepack | 13 August 2012 |
| 15 tablet, film coated, extended release in 1 bottle | 63629-4483-7 | Bryant Ranch Prepack | 29 April 2014 |
| 20 tablet, film coated, extended release in 1 bottle | 63629-4483-8 | Bryant Ranch Prepack | 3 January 2022 |
| 84 tablet, film coated, extended release in 1 bottle | 63629-4483-9 | Bryant Ranch Prepack | 15 April 2015 |
| 26 tablet, film coated, extended release in 1 bottle | 71335-0736-0 | Bryant Ranch Prepack | 3 April 2024 |
| 30 tablet, film coated, extended release in 1 bottle | 71335-0736-1 | Bryant Ranch Prepack | 16 March 2018 |
| 60 tablet, film coated, extended release in 1 bottle | 71335-0736-2 | Bryant Ranch Prepack | 28 March 2018 |
| 90 tablet, film coated, extended release in 1 bottle | 71335-0736-3 | Bryant Ranch Prepack | 13 April 2018 |
| 120 tablet, film coated, extended release in 1 bottle | 71335-0736-4 | Bryant Ranch Prepack | 3 April 2024 |
| 40 tablet, film coated, extended release in 1 bottle | 71335-0736-5 | Bryant Ranch Prepack | 3 April 2024 |
| 14 tablet, film coated, extended release in 1 bottle | 71335-0736-6 | Bryant Ranch Prepack | 3 April 2024 |
| 15 tablet, film coated, extended release in 1 bottle | 71335-0736-7 | Bryant Ranch Prepack | 3 April 2024 |
| 20 tablet, film coated, extended release in 1 bottle | 71335-0736-8 | Bryant Ranch Prepack | 3 April 2024 |
| 84 tablet, film coated, extended release in 1 bottle | 71335-0736-9 | Bryant Ranch Prepack | 3 April 2024 |
| 100 tablet, film coated, extended release in 1 bottle | 72162-1789-1 | Bryant Ranch Prepack | 11 May 2012 |
| 30 tablet, film coated, extended release in 1 bottle | 72162-1789-3 | Bryant Ranch Prepack | 11 May 2012 |
| 60 tablet, film coated, extended release in 1 bottle | 72162-1789-6 | Bryant Ranch Prepack | 11 May 2012 |
| 90 tablet, film coated, extended release in 1 bottle | 72162-1789-9 | Bryant Ranch Prepack | 11 May 2012 |
| 100 blister pack in 1 box, unit-dose / 1 tablet, film coated, extended release in 1 blister pack | 68084-157-01 | American Health Packaging | 5 November 2013 |
| 100 blister pack in 1 carton / 1 tablet, film coated, extended release in 1 blister pack | 0904-6557-61 | Major Pharmaceuticals | 14 January 2011 |
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 18 September 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 Morphine 15 mg extended-release tablet.
Other strengths and forms of Morphine
Clinical summary
Morphine is an opioid agonist indicated only for intrathecal or epidural infusion in the management of intractable chronic pain severe enough to require an opioid analgesic and for which less invasive means of controlling pain are inadequate. MedsAcross supplies Morphine 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 MorphineFor healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.
Data sources
- DailyMed label record · Checked 12 November 2026
- INFUMORPH 200 prescribing information (Hikma Pharmaceuticals) · U.S. National Library of Medicine, DailyMed
Need Morphine 15 mg extended-release tablet for your hospital or patient?
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