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01 1Ajinomoto Co., Inc.

02 1Divi's Laboratories Limited

03 1Hetero Drugs Limited

04 1Maithri Drugs Private Limited

05 1Professional Compounding Centers of America dba PCCA

06 2Shandong Xinhua Pharmaceutical Company Limited

07 1Spectrum Laboratory Products, Inc.

08 2Teva Pharmaceutical Works Private Limited Company

09 1ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD.

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PharmaCompass

01

The Generic Rx Session
Not Confirmed
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The Generic Rx Session
Not Confirmed

LEVODOPA

NDC Package Code : 17333-059

Start Marketing Date : 1982-04-15

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

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02

BioAsia
Not Confirmed
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03

The Generic Rx Session
Not Confirmed
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The Generic Rx Session
Not Confirmed

LEVODOPA

NDC Package Code : 65977-0126

Start Marketing Date : 1982-01-01

End Marketing Date : 2024-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

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04

The Generic Rx Session
Not Confirmed
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The Generic Rx Session
Not Confirmed

LEVODOPA

NDC Package Code : 51927-0049

Start Marketing Date : 2020-05-18

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT FOR HUMAN P...

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05

BioAsia
Not Confirmed
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BioAsia
Not Confirmed

LEVODOPA

NDC Package Code : 58624-0238

Start Marketing Date : 2000-01-01

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

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06

BioAsia
Not Confirmed
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BioAsia
Not Confirmed

LEVODOPA

NDC Package Code : 58624-0234

Start Marketing Date : 2000-01-01

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

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07

The Generic Rx Session
Not Confirmed
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The Generic Rx Session
Not Confirmed

LEVODOPA

NDC Package Code : 49452-2680

Start Marketing Date : 1990-04-01

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1g/g)

Marketing Category : BULK INGREDIENT

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08

BioAsia
Not Confirmed
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BioAsia
Not Confirmed

LEVODOPA

NDC Package Code : 51846-1052

Start Marketing Date : 2012-04-12

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (100kg/100kg)

Marketing Category : BULK INGREDIENT

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09

BioAsia
Not Confirmed
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BioAsia
Not Confirmed

LEVODOPA

NDC Package Code : 51846-1053

Start Marketing Date : 2012-08-16

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (100kg/100kg)

Marketing Category : BULK INGREDIENT

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10

The Generic Rx Session
Not Confirmed
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The Generic Rx Session
Not Confirmed

LEVODOPA

NDC Package Code : 64220-199

Start Marketing Date : 2018-03-27

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

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Looking for 59-92-7 / Etilevodopa API manufacturers, exporters & distributors?

Etilevodopa manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Etilevodopa API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Etilevodopa manufacturer or Etilevodopa supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Etilevodopa manufacturer or Etilevodopa supplier.

PharmaCompass also assists you with knowing the Etilevodopa API Price utilized in the formulation of products. Etilevodopa API Price is not always fixed or binding as the Etilevodopa Price is obtained through a variety of data sources. The Etilevodopa Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Etilevodopa

Synonyms

L-dopa, 59-92-7, Dopar, 3,4-dihydroxy-l-phenylalanine, 3-hydroxy-l-tyrosine, Bendopa

Cas Number

59-92-7

Unique Ingredient Identifier (UNII)

46627O600J

About Etilevodopa

The naturally occurring form of DIHYDROXYPHENYLALANINE and the immediate precursor of DOPAMINE. Unlike dopamine itself, it can be taken orally and crosses the blood-brain barrier. It is rapidly taken up by dopaminergic neurons and converted to DOPAMINE. It is used for the treatment of PARKINSONIAN DISORDERS and is usually given with agents that inhibit its conversion to dopamine outside of the central nervous system.

Levodopa Manufacturers

A Levodopa manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Levodopa, including repackagers and relabelers. The FDA regulates Levodopa manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Levodopa API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

click here to find a list of Levodopa manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Levodopa Suppliers

A Levodopa supplier is an individual or a company that provides Levodopa active pharmaceutical ingredient (API) or Levodopa finished formulations upon request. The Levodopa suppliers may include Levodopa API manufacturers, exporters, distributors and traders.

click here to find a list of Levodopa suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Levodopa NDC

National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Levodopa as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Levodopa API and other APIs are published in this directory by the FDA.

Unfinished drugs

The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.

Pharmaceutical companies that manufacture Levodopa as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain Levodopa and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Levodopa NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Levodopa suppliers with NDC on PharmaCompass.

Levodopa Manufacturers | Traders | Suppliers

Levodopa Manufacturers, Traders, Suppliers 1
Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.