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01 1Veranova, L.P.

02 1Noramco, LLC

03 4Cambrex Charles City, Inc

04 1Chattem Chemicals, Inc.

05 1Curia Missouri, Inc.

06 2Janssen Pharmaceutical Sciences Unlimited Company

07 1Medisca Inc.

08 1Professional Compounding Center of America

09 1Professional Compounding Centers of America

10 2S&B Pharma LLC dba Norac Pharma

11 1Siegfried USA, LLC

12 5SpecGx LLC

13 1Spectrum Laboratory Products, Inc.

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PharmaCompass

01

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The Generic Rx Session
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothVeranova: A CDMO that manages complexity with confidence.

METHYLPHENIDATE HYDROCHLORIDE

NDC Package Code : 49812-0020

Start Marketing Date : 2010-06-01

End Marketing Date : 2024-12-31

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

Marketing Category : BULK INGREDIENT

Veranova

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothNoramco is a partner to the pharmaceutical industry for controlled substance development & manufacturing.

METHYLPHENIDATE HYDROCHLORIDE

NDC Package Code : 51634-0114

Start Marketing Date : 2017-07-31

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

Noramco

03

The Generic Rx Session
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04

The Generic Rx Session
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The Generic Rx Session
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METHYLPHENIDATE HYDROCHLORIDE

NDC Package Code : 0406-0570

Start Marketing Date : 2014-01-01

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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05

The Generic Rx Session
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The Generic Rx Session
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METHYLPHENIDATE HYDROCHLORIDE

NDC Package Code : 0406-1335

Start Marketing Date : 2014-03-01

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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06

The Generic Rx Session
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The Generic Rx Session
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METHYLPHENIDATE HYDROCHLORIDE

NDC Package Code : 0406-1571

Start Marketing Date : 1996-12-30

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
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The Generic Rx Session
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METHYLPHENIDATE HYDROCHLORIDE

NDC Package Code : 0406-2069

Start Marketing Date : 1999-07-07

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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08

The Generic Rx Session
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The Generic Rx Session
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METHYLPHENIDATE HYDROCHLORIDE

NDC Package Code : 0406-8335

Start Marketing Date : 2003-06-30

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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09

The Generic Rx Session
Not Confirmed
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The Generic Rx Session
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METHYLPHENIDATE HYDROCHLORIDE

NDC Package Code : 38779-0851

Start Marketing Date : 2014-05-26

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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10

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Looking for 298-59-9 / Methylphenidate Hydrochloride API manufacturers, exporters & distributors?

Methylphenidate Hydrochloride manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Methylphenidate Hydrochloride 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 Methylphenidate Hydrochloride manufacturer or Methylphenidate Hydrochloride supplier for your needs.

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

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

API | Excipient name

Methylphenidate Hydrochloride

Synonyms

298-59-9, Centedrin, Centedrine, Methylphenidate hcl, Concerta, Ritalin

Cas Number

298-59-9

About Methylphenidate Hydrochloride

A central nervous system stimulant used most commonly in the treatment of ATTENTION DEFICIT DISORDER in children and for NARCOLEPSY. Its mechanisms appear to be similar to those of DEXTROAMPHETAMINE. The d-isomer of this drug is referred to as DEXMETHYLPHENIDATE HYDROCHLORIDE.

Ritalin Manufacturers

A Ritalin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ritalin, including repackagers and relabelers. The FDA regulates Ritalin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ritalin 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 Ritalin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Ritalin Suppliers

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

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

Ritalin 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 Ritalin as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Ritalin 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 Ritalin 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 Ritalin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Ritalin NDC to their finished compounded human drug products, they may choose to do so.

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

Ritalin Manufacturers | Traders | Suppliers

Ritalin 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.