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Medicine

Rivastigmine 4.6 mg/24 hours transdermal patch

Rivastigmine · Transdermal
Available on requestPrescription onlyUS FDAGeneric name

Rivastigmine 4.6 mg/24 hours transdermal patch is a generic prescription medicine for transdermal 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

Available on request

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 to 15°C to 30°C (59°F to 86°F).

Key facts

Active ingredient (INN)
Rivastigmine
Brand
Sold under the generic name
Strength
4.6 mg/24 hours
Dosage form
Transdermal patch
Route
Transdermal
Packs
30 pouches, 30 patches and 5 more
Manufacturers
Zydus LifesciencesIndiaBryant Ranch PrepackAmneal PharmaceuticalsBreckenridge PharmaceuticalMylan PharmaceuticalsSandoz
Origin register
US FDA, United States
Storage
Store at 25°C (77°F), excursions permitted to 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
N06DA03 Rivastigmine
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
30 June 2015
Identifiers
RxCUI 725021, 725023, 1308569DailyMed set ID b201fe68-b5e5-4a6f-8cf1-069543f03e76, 8b671fc9-8cb0-4406-a9ee-7c95086d6200, 92a58ebb-748d-49f4-bf11-ecbcf5424152 +5NDC 51991-897, 65162-825, 0781-7304 +5Application ANDA209063, ANDA207308, NDA022083 +2

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.

PackCodeLabelerMarketed since
30 pouch in 1 carton / 24 h in 1 pouch70710-1196-7Zydus LifesciencesIndia6 March 2019
30 pouch in 1 carton / 24 h in 1 pouch70771-1949-7Zydus LifesciencesIndia6 March 2019
30 patch in 1 carton / 24 h in 1 patch65162-825-34Amneal Pharmaceuticals30 June 2015
30 pouch in 1 carton / 1 patch in 1 pouch / 24 h in 1 patch51991-897-30Breckenridge Pharmaceutical19 December 2019
30 pouch in 1 carton / 1 patch in 1 pouch / 24 h in 1 patch0378-9070-93Mylan Pharmaceuticals20 June 2018
30 patch in 1 carton / 24 h in 1 patch0781-7304-31Sandoz2 September 2015
30 pouch in 1 carton / 1 patch in 1 pouch / 24 h in 1 patch63629-2065-1Bryant Ranch Prepack11 February 2021
30 pouch in 1 carton / 1 patch in 1 pouch / 24 h in 1 patch72162-1608-3Bryant Ranch Prepack19 December 2019

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.

RegisterStatusSource
US FDAListed, marketedSource record for this pageChecked 12 November 2026
US FDAFirst approved 21 April 2000Drugs@FDA
EU (EMA)AuthorisedEMA medicines data
India (CDSCO)Not yet confirmed against CDSCO approval lists—
AustriaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
BelgiumRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
BulgariaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
CroatiaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
CyprusRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
CzechiaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
DenmarkRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
EstoniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
FinlandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
FranceRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
GermanyRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
GreeceRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
HungaryRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
IcelandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
IrelandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
ItalyRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LatviaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LiechtensteinRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LithuaniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LuxembourgRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
MaltaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
NetherlandsRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
NorwayRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
PolandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
PortugalRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
RomaniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SlovakiaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SloveniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SpainRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SwedenRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
United StatesRegisteredUS 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 Rivastigmine 4.6 mg/24 hours transdermal patch.

Compare 1

Other strengths and forms of Rivastigmine

Clinical summary

Rivastigmine is a cholinesterase inhibitor indicated for treatment of mild, moderate, and severe dementia of the Alzheimer’s type (AD), among other approved uses. It is available as capsules and transdermal patches for oral use. MedsAcross supplies Rivastigmine 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 Rivastigmine

For healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.

Data sources

Need Rivastigmine 4.6 mg/24 hours transdermal patch 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.