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Medicine

Carbidopa and Levodopa 25 mg/250 mg tablet

Available on requestPrescription onlyUS FDAGeneric name

Carbidopa and Levodopa 25 mg/250 mg tablet is a generic prescription medicine for oral use, made by 19 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 20º to 25ºC (68º to 77ºF), excursions permitted to 15° to 30°C (59°…

Key facts

Active ingredient (INN)
Carbidopa and Levodopa
Brand
Sold under the generic name
Strength
25 mg/250 mg
Dosage form
Tablet
Route
Oral
Packs
100 tablets, 500 tablets, 1000 tablets and 48 more
Manufacturers
Aurobindo PharmaIndiaCamber PharmaceuticalsIndiaDr. Reddy's LaboratoriesIndiaSun Pharmaceutical IndustriesIndiaAdvagen PharmaBryant Ranch PrepackScieGen PharmaceuticalsCouplerTeva PharmaceuticalsTruPharma19 labelers on the register
Origin register
US FDA, United States
Storage
Store at 20º to 25ºC (68º to 77ºF), excursions permitted to 15° to 30°C (59° to 86°F). Store in a tightly closed container, protected from light and moisture.
Cold chain
Not required on record
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
N04BA02 Carbidopa and Levodopa
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
7 May 2021
Identifiers
RxCUI 197443, 197444, 197445DailyMed set ID 770ba054-fec4-4833-8096-85c3ce3ae830, 0c630a24-dc51-4601-a5d6-2f9e397a0449, 11e706c4-433c-1ea6-e063-6294a90ad360 +19NDC 31722-383, 72865-363, 42291-488 +19Application ANDA218939, ANDA074260, ANDA073607 +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 19 labelers. The register lists 51 packs for this generic presentation, and we confirm the exact pack on the quote.

PackCodeLabelerMarketed since
100 tablet in 1 bottle59651-458-01Aurobindo PharmaIndia28 November 2022
500 tablet in 1 bottle59651-458-05Aurobindo PharmaIndia28 November 2022
1000 tablet in 1 bottle59651-458-99Aurobindo PharmaIndia28 November 2022
100 tablet in 1 bottle31722-383-01Camber PharmaceuticalsIndia27 May 2025
500 tablet in 1 bottle31722-383-05Camber PharmaceuticalsIndia27 May 2025
1000 tablet in 1 bottle31722-383-10Camber PharmaceuticalsIndia27 May 2025
100 tablet in 1 bottle75907-021-01Dr. Reddy's LaboratoriesIndia1 May 2024
500 tablet in 1 bottle75907-021-05Dr. Reddy's LaboratoriesIndia15 March 2025
100 tablet in 1 bottle62756-985-01Sun Pharmaceutical IndustriesIndia12 August 2021
500 tablet in 1 bottle62756-985-02Sun Pharmaceutical IndustriesIndia12 August 2021
1000 tablet in 1 bottle72888-108-00Advagen Pharma1 April 2023
100 tablet in 1 bottle72888-108-01Advagen Pharma1 April 2023
500 tablet in 1 bottle72888-108-05Advagen Pharma1 April 2023
30 tablet in 1 bottle72888-108-30Advagen Pharma1 April 2023
100 tablet in 1 bottle50228-459-01ScieGen Pharmaceuticals7 May 2021
500 tablet in 1 bottle50228-459-05ScieGen Pharmaceuticals7 May 2021
1000 tablet in 1 bottle50228-459-10ScieGen Pharmaceuticals7 May 2021
30 tablet in 1 bottle50228-459-30ScieGen Pharmaceuticals7 May 2021
100 tablet in 1 bottle0093-9703-01Teva Pharmaceuticals5 March 2024
500 tablet in 1 bottle0093-9703-05Teva Pharmaceuticals15 December 2023
1000 tablet in 1 bottle0093-9703-10Teva Pharmaceuticals8 February 2024
1000 tablet in 1 bottle52817-392-00TruPharma4 April 2023
100 tablet in 1 bottle52817-392-10TruPharma4 April 2023
500 tablet in 1 bottle52817-392-50TruPharma4 April 2023
100 tablet in 1 bottle72865-363-01XLCare Pharmaceuticals19 January 2026
1000 tablet in 1 bottle72865-363-10XLCare Pharmaceuticals19 January 2026
30 tablet in 1 blister pack67046-1450-3Coupler7 February 2025
30 tablet in 1 blister pack67046-1668-3Coupler22 April 2026
30 tablet in 1 blister pack67046-1689-3Coupler13 July 2026
30 tablet in 1 bottle63629-4134-1Bryant Ranch Prepack7 April 2025
270 tablet in 1 bottle63629-4134-2Bryant Ranch Prepack7 April 2025
60 tablet in 1 bottle63629-4134-3Bryant Ranch Prepack7 April 2025
100 tablet in 1 bottle63629-9154-1Bryant Ranch Prepack27 January 2022
100 blister pack in 1 carton / 1 tablet in 1 blister pack60687-836-01American Health Packaging16 March 2024
100 tablet in 1 bottle42291-488-01AvKARE21 February 2024
1000 tablet in 1 bottle42291-488-10AvKARE21 February 2024
10 blister pack in 1 bag / 1 tablet in 1 blister pack55154-0192-0Cardinal Health10 October 2025
100 blister pack in 1 carton / 1 tablet in 1 blister pack0904-7549-61Major Pharmaceuticals28 April 2025
100 tablet in 1 bottle, plastic71205-879-00Proficient Rx5 November 2021
1000 tablet in 1 bottle, plastic71205-879-11Proficient Rx5 November 2021

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 2 May 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 Carbidopa and Levodopa

Clinical summary

Carbidopa and Levodopa is a fixed-dose combination medicine indicated in the treatment of Parkinson's disease, post-encephalitic parkinsonism, and symptomatic parkinsonism that may follow carbon monoxide intoxication or manganese intoxication. MedsAcross supplies Carbidopa and Levodopa 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 Carbidopa and Levodopa

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

Data sources

Need Carbidopa and Levodopa 25 mg/250 mg 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.