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Medicine

Oxybutynin 10 mg extended-release tablet

Oxybutynin · Oral
Available on requestPrescription onlyUS FDAGeneric name

Oxybutynin 10 mg extended-release tablet is a generic prescription medicine for oral use, made by 18 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)
Oxybutynin
Brand
Sold under the generic name
Strength
10 mg
Dosage form
Extended-release tablet
Route
Oral
Packs
100 tablets, 500 tablets, 30 tablets and 50 more
Manufacturers
Zydus LifesciencesIndiaAccord HealthcareIndiaAjanta PharmaIndiaBryant Ranch PrepackAmneal PharmaceuticalsA-S Medication SolutionsPD-Rx PharmaceuticalsAdvagen PharmaLannettRising Pharma Holdings18 labelers on the register
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). Protect from moisture and humidity.
Cold chain
Not required on record
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
G04BD04 Oxybutynin
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
1 March 2009
Identifiers
RxCUI 863619, 863628, 863636DailyMed set ID 88f08450-559e-4038-aad1-051e4ab283cf, ada3be87-2cdd-75f7-e053-2995a90aa95b, a1f8be75-2eb9-4eef-8fb4-144ef2bf7ae1 +22NDC 71205-667, 72189-132, 72789-049 +22Application ANDA207138, ANDA078503, ANDA202332 +4

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

A sample of 40 packs from 18 labelers. The register lists 53 packs for this generic presentation, and we confirm the exact pack on the quote.

PackCodeLabelerMarketed since
100 tablet, film coated, extended release in 1 bottle68382-256-01Zydus LifesciencesIndia10 August 2017
500 tablet, film coated, extended release in 1 bottle68382-256-05Zydus LifesciencesIndia10 August 2017
30 tablet, film coated, extended release in 1 bottle68382-256-06Zydus LifesciencesIndia10 August 2017
60 tablet, film coated, extended release in 1 bottle68382-256-14Zydus LifesciencesIndia10 August 2017
90 tablet, film coated, extended release in 1 bottle68382-256-16Zydus LifesciencesIndia10 August 2017
10 blister pack in 1 carton / 10 tablet, film coated, extended release in 1 blister pack68382-256-77Zydus LifesciencesIndia10 August 2017
100 tablet, film coated, extended release in 1 bottle70771-1087-1Zydus LifesciencesIndia10 August 2017
30 tablet, film coated, extended release in 1 bottle70771-1087-3Zydus LifesciencesIndia10 August 2017
10 blister pack in 1 carton / 10 tablet, film coated, extended release in 1 blister pack70771-1087-4Zydus LifesciencesIndia10 August 2017
500 tablet, film coated, extended release in 1 bottle70771-1087-5Zydus LifesciencesIndia10 August 2017
60 tablet, film coated, extended release in 1 bottle70771-1087-6Zydus LifesciencesIndia10 August 2017
90 tablet, film coated, extended release in 1 bottle70771-1087-9Zydus LifesciencesIndia10 August 2017
100 tablet, extended release in 1 bottle16729-318-01Accord HealthcareIndia20 December 2016
500 tablet, extended release in 1 bottle16729-318-16Accord HealthcareIndia17 April 2017
100 tablet, extended release in 1 bottle27241-156-04Ajanta PharmaIndia28 February 2019
500 tablet, extended release in 1 bottle27241-156-08Ajanta PharmaIndia28 February 2019
100 tablet, extended release in 1 bottle72888-031-01Advagen Pharma27 October 2020
500 tablet, extended release in 1 bottle72888-031-05Advagen Pharma10 July 2024
30 tablet, extended release in 1 bottle65162-372-03Amneal Pharmaceuticals2 November 2015
90 tablet, extended release in 1 bottle65162-372-09Amneal Pharmaceuticals2 November 2015
100 tablet, extended release in 1 bottle65162-372-10Amneal Pharmaceuticals2 November 2015
500 tablet, extended release in 1 bottle65162-372-50Amneal Pharmaceuticals2 November 2015
90 tablet, extended release in 1 bottle62135-508-90Chartwell RX3 March 2023
100 tablet, extended release in 1 bottle62175-271-37Lannett1 March 2009
500 tablet, extended release in 1 bottle62175-271-41Lannett1 March 2009
100 tablet, extended release in 1 bottle64980-210-01Rising Pharma Holdings27 September 2016
500 tablet, extended release in 1 bottle64980-210-05Rising Pharma Holdings29 March 2022
90 tablet, extended release in 1 bottle50090-4307-0A-S Medication Solutions23 May 2019
90 tablet, film coated, extended release in 1 bottle50090-5353-0A-S Medication Solutions11 November 2020
90 tablet, extended release in 1 bottle50090-6673-0A-S Medication Solutions1 September 2023
90 tablet, extended release in 1 bottle, plastic43063-790-90PD-Rx Pharmaceuticals21 September 2017
90 tablet, extended release in 1 bottle, plastic72789-049-90PD-Rx Pharmaceuticals28 January 2020
90 tablet, extended release in 1 bottle, plastic72789-414-90PD-Rx Pharmaceuticals11 June 2024
30 tablet, extended release in 1 bottle71335-1690-1Bryant Ranch Prepack29 December 2021
18 tablet, extended release in 1 bottle71335-1690-2Bryant Ranch Prepack29 December 2021
90 tablet, extended release in 1 bottle71335-1690-3Bryant Ranch Prepack11 August 2020
60 tablet, extended release in 1 bottle71335-1690-4Bryant Ranch Prepack29 December 2021
30 tablet, extended release in 1 bottle71335-2121-1Bryant Ranch Prepack20 June 2022
18 tablet, extended release in 1 bottle71335-2121-2Bryant Ranch Prepack20 June 2022
90 tablet, extended release in 1 bottle71335-2121-3Bryant Ranch Prepack20 June 2022

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 16 July 1975Drugs@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

Other strengths and forms of Oxybutynin

Clinical summary

Oxybutynin is a cholinergic muscarinic antagonist indicated for the treatment of overactive bladder in men with symptoms of urge urinary incontinence, urgency, and frequency. It is available as extended-release tablets, tablets and oral solution for transdermal use. MedsAcross supplies Oxybutynin 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 Oxybutynin

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

Data sources

Need Oxybutynin 10 mg extended-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.