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01 1Symbiotec Pharmalab Private Limited

02 3Farmabios S.p.A.

03 1Curia Spain S.A.U.

04 1Fagron Services BV

05 1Galenova Inc

06 2HENAN LIHUA PHARMACEUTICAL CO., LTD.

07 1LETCO MEDICAL, LLC

08 1Medisca Inc.

09 1NEWCHEM SPA

10 1Professional Compounding Centers of America dba PCCA

11 1SYMBIOTICA SPECIALITY INGREDIENTS SDN.BHD

12 1Sicor S.r.l.

13 1Xenex Laboratories Inc

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSymbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.

CLOBETASOL PROPIONATE

NDC Package Code : 22552-0006

Start Marketing Date : 2017-12-13

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

Symbiotec Pharmalab

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothAxplora is your partner of choice for complex APIs.

CLOBETASOL PROPIONATE

NDC Package Code : 46439-8708

Start Marketing Date : 2000-10-09

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

Axplora CB

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothAxplora is your partner of choice for complex APIs.

CLOBETASOL PROPIONATE

NDC Package Code : 46439-8784

Start Marketing Date : 2025-02-20

End Marketing Date : 2026-12-31

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

Marketing Category : BULK INGREDIENT

Axplora CB

04

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothAxplora is your partner of choice for complex APIs.

CLOBETASOL PROPIONATE

NDC Package Code : 46439-8747

Start Marketing Date : 2000-10-09

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

Axplora CB

05

Cophex
Not Confirmed
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Cophex
Not Confirmed

CLOBETASOL PROPIONATE

NDC Package Code : 62991-1492

Start Marketing Date : 2011-03-05

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT FOR HUMAN P...

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06

Cophex
Not Confirmed
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Cophex
Not Confirmed

CLOBETASOL PROPIONATE

NDC Package Code : 38779-0372

Start Marketing Date : 2014-08-25

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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07

Cophex
Not Confirmed
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08

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Cophex
Not Confirmed

CLOBETASOL PROPIONATE

NDC Package Code : 51927-2627

Start Marketing Date : 2013-06-24

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT FOR HUMAN P...

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09

Cophex
Not Confirmed
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Cophex
Not Confirmed

CLOBETASOL PROPIONATE

NDC Package Code : 53183-0446

Start Marketing Date : 2017-11-21

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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Looking for 25122-46-7 / Clobetasol Propionate API manufacturers, exporters & distributors?

Clobetasol Propionate manufacturers, exporters & distributors 1

65

PharmaCompass offers a list of Clobetasol Propionate 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 Clobetasol Propionate manufacturer or Clobetasol Propionate supplier for your needs.

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

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

API | Excipient name

Clobetasol Propionate

Synonyms

25122-46-7, Clobetasol 17-propionate, Clobex, Dermovate, Temovate, Embeline

Cas Number

25122-46-7

Unique Ingredient Identifier (UNII)

779619577M

About Clobetasol Propionate

A derivative of PREDNISOLONE with high glucocorticoid activity and low mineralocorticoid activity. Absorbed through the skin faster than FLUOCINONIDE, it is used topically in treatment of PSORIASIS but may cause marked adrenocortical suppression.

Dermovate Manufacturers

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

Dermovate Suppliers

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

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

Dermovate 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 Dermovate as an active pharmaceutical ingredient (API).

Finished drug products

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

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

Dermovate Manufacturers | Traders | Suppliers

Dermovate Manufacturers, Traders, Suppliers 1
32

We have 13 companies offering Dermovate

Get in contact with the supplier of your choice:

  1. Axplora
  2. Symbiotec Pharmalab
  3. Curia
  4. Fagron Group
  5. Galenova
  6. Henan Lihua Pharmaceutical
  7. Letco Medical
  8. Medisca
  9. NEWCHEM SPA
  10. Pcca
  11. Sicor
  12. Symbiotica
  13. Xenex Labs
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.