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01 1Supriya Lifescience Limited

02 1Malladi Drugs & Pharmaceuticals Limited

03 1AZEEMA PHARMA INC

04 2Aurobindo Pharma Limited

05 1Dasami Lab Private Limited

06 1Divi's Laboratories Limited

07 1Exemed Pharmaceuticals

08 1LETCO MEDICAL, LLC

09 1Medisca Inc.

10 1Professional Compounding Centers of America

11 1QIDONG DONGYUE PHARMACEUTICAL CO., LTD.

12 1Spectrum Laboratory Products, Inc.

13 1Srini Pharmaceuticals Private Limited

14 1Vasudha Pharma Chem Limited

15 1Wanbury Limited

16 1Zhejiang Apeloa Kangyu Pharmaceutical Co., Ltd.

17 1Zhejiang Bamboo Pharmaceuticals Co.,Ltd

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSupriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.

DEXTROMETHORPHAN HYDROBROMIDE

NDC Package Code : 61281-6500

Start Marketing Date : 2017-01-31

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

Supriya

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothMalladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.

DEXTROMETHORPHAN HYDROBROMIDE

NDC Package Code : 57218-760

Start Marketing Date : 2017-02-28

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

Malladi

03

Cophex
Not Confirmed
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05

Cophex
Not Confirmed
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Cophex
Not Confirmed

DEXTROMETHORPHAN HYDROBROMIDE

NDC Package Code : 60155-002

Start Marketing Date : 2020-07-20

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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06

Cophex
Not Confirmed
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Cophex
Not Confirmed

DEXTROMETHORPHAN HYDROBROMIDE

NDC Package Code : 62991-1042

Start Marketing Date : 2011-10-12

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT FOR HUMAN P...

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07

Cophex
Not Confirmed
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Cophex
Not Confirmed

DEXTROMETHORPHAN HYDROBROMIDE

NDC Package Code : 38779-0355

Start Marketing Date : 2015-03-30

End Marketing Date : 2026-12-31

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

Marketing Category : BULK INGREDIENT FOR HUMAN P...

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08

arrow
Cophex
Not Confirmed

DEXTROMETHORPHAN HYDROBROMIDE

NDC Package Code : 51927-0260

Start Marketing Date : 2022-11-21

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT FOR HUMAN P...

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10

Cophex
Not Confirmed
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Cophex
Not Confirmed

DEXTROMETHORPHAN HYDROBROMIDE

NDC Package Code : 62350-0081

Start Marketing Date : 2019-08-29

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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Looking for 125-69-9 / Dextromethorphan Hydrobromide API manufacturers, exporters & distributors?

Dextromethorphan Hydrobromide manufacturers, exporters & distributors 1

65

PharmaCompass offers a list of Dextromethorphan Hydrobromide 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 Dextromethorphan Hydrobromide manufacturer or Dextromethorphan Hydrobromide supplier for your needs.

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

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

API | Excipient name

Dextromethorphan Hydrobromide

Synonyms

125-69-9, Antussan, Demorphan, Dormethan, Metrorat, Medicon

Cas Number

125-69-9

Unique Ingredient Identifier (UNII)

Z0CG3115FG

About Dextromethorphan Hydrobromide

Methyl analog of DEXTRORPHAN that shows high affinity binding to several regions of the brain, including the medullary cough center. This compound is an NMDA receptor antagonist (RECEPTORS, N-METHYL-D-ASPARTATE) and acts as a non-competitive channel blocker. It is one of the widely used ANTITUSSIVES, and is also used to study the involvement of glutamate receptors in neurotoxicity.

Romilar Manufacturers

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

Romilar Suppliers

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

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

Romilar 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 Romilar as an active pharmaceutical ingredient (API).

Finished drug products

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

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

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.