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Medicine

Carbidopa and Levodopa 10 mg/100 mg tablet

Available on requestPrescription onlyUS FDAGeneric name

Carbidopa and Levodopa 10 mg/100 mg tablet is a generic prescription medicine for oral use, made by 16 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°-30°C (59°-86°F). Protect…

Key facts

Active ingredient (INN)
Carbidopa and Levodopa
Brand
Sold under the generic name
Strength
10 mg/100 mg
Dosage form
Tablet
Route
Oral
Packs
100 tablets, 500 tablets, 1000 tablets and 39 more
Manufacturers
Sun Pharmaceutical IndustriesIndiaAurobindo PharmaIndiaCamber PharmaceuticalsIndiaDr. Reddy's LaboratoriesIndiaProficient RxAdvagen PharmaScieGen PharmaceuticalsA-S Medication SolutionsAvKARETeva Pharmaceuticals16 labelers on the register
Origin register
US FDA, United States
Storage
Store at 25°C (77°F), excursions permitted to 15°-30°C (59°-86°F). Protect 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
28 October 2008
Identifiers
RxCUI 197443, 197444, 197445DailyMed set ID 87ab55c9-203d-d595-3e3e-0e38f2f6d9c4, 45909de3-0852-4e61-8a9e-23f8fcc2463a, 4ace5274-b6cf-414c-b9c0-f60e28a9cea5 +13NDC 75907-022, 0615-8555, 0093-9701 +13Application ANDA073618, ANDA074260, ANDA216505 +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 16 labelers. The register lists 42 packs for this generic presentation, and we confirm the exact pack on the quote.

PackCodeLabelerMarketed since
100 tablet in 1 bottle59651-456-01Aurobindo PharmaIndia28 November 2022
500 tablet in 1 bottle59651-456-05Aurobindo PharmaIndia28 November 2022
100 tablet in 1 bottle31722-381-01Camber PharmaceuticalsIndia27 May 2025
500 tablet in 1 bottle31722-381-05Camber PharmaceuticalsIndia27 May 2025
100 tablet in 1 bottle75907-022-01Dr. Reddy's LaboratoriesIndia1 May 2024
100 tablet in 1 bottle62756-517-08Sun Pharmaceutical IndustriesIndia28 October 2008
500 tablet in 1 bottle62756-517-13Sun Pharmaceutical IndustriesIndia28 October 2008
1000 tablet in 1 bottle62756-517-18Sun Pharmaceutical IndustriesIndia28 October 2008
30 tablet in 1 bottle62756-517-83Sun Pharmaceutical IndustriesIndia28 October 2008
100 tablet in 1 bottle62756-517-88Sun Pharmaceutical IndustriesIndia28 October 2008
1000 tablet in 1 bottle72888-106-00Advagen Pharma1 February 2023
100 tablet in 1 bottle72888-106-01Advagen Pharma1 February 2023
500 tablet in 1 bottle72888-106-05Advagen Pharma1 February 2023
30 tablet in 1 bottle72888-106-30Advagen Pharma1 February 2023
100 tablet in 1 bottle50228-457-01ScieGen Pharmaceuticals7 May 2021
500 tablet in 1 bottle50228-457-05ScieGen Pharmaceuticals7 May 2021
1000 tablet in 1 bottle50228-457-10ScieGen Pharmaceuticals7 May 2021
30 tablet in 1 bottle50228-457-30ScieGen Pharmaceuticals7 May 2021
100 tablet in 1 bottle0093-9701-01Teva Pharmaceuticals18 January 2022
500 tablet in 1 bottle0093-9701-05Teva Pharmaceuticals14 June 2022
100 tablet in 1 bottle52817-390-10TruPharma4 April 2023
500 tablet in 1 bottle52817-390-50TruPharma4 April 2023
100 tablet in 1 bottle72865-361-01XLCare Pharmaceuticals19 January 2026
1000 tablet in 1 bottle72865-361-10XLCare Pharmaceuticals19 January 2026
30 tablet in 1 bottle50090-7186-0A-S Medication Solutions26 June 2024
90 tablet in 1 bottle50090-7186-1A-S Medication Solutions26 June 2024
30 blister pack in 1 carton / 1 tablet in 1 blister pack68002-100-04American Health Packaging28 July 2025
100 tablet in 1 bottle42291-471-01AvKARE24 June 2022
500 tablet in 1 bottle42291-471-50AvKARE24 June 2022
30 tablet in 1 blister pack67046-1614-3Coupler17 November 2025
100 tablet in 1 bottle, plastic71205-877-00Proficient Rx5 November 2021
1000 tablet in 1 bottle, plastic71205-877-11Proficient Rx5 November 2021
30 tablet in 1 bottle, plastic71205-877-30Proficient Rx5 November 2021
500 tablet in 1 bottle, plastic71205-877-55Proficient Rx5 November 2021
60 tablet in 1 bottle, plastic71205-877-60Proficient Rx5 November 2021
240 tablet in 1 bottle, plastic71205-877-64Proficient Rx5 November 2021
120 tablet in 1 bottle, plastic71205-877-72Proficient Rx5 November 2021
180 tablet in 1 bottle, plastic71205-877-78Proficient Rx5 November 2021
90 tablet in 1 bottle, plastic71205-877-90Proficient Rx5 November 2021
30 tablet in 1 blister pack0615-8555-39Vangard Labs24 October 2024

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

Alternatives

Other makers and brands of Carbidopa and Levodopa 10 mg/100 mg tablet.

Compare 1

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 10 mg/100 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.