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01 2PCAS

02 4Willow Birch Pharma, LLC

03 1Excella GmbH & Co. KG

04 2ALMON HEALTHCARE PRIVATE LIMITED

05 1ASG Biochem Private Limited

06 2AX Pharmaceutical Corp

07 3Almon Healthcare Private Limited

08 1BILLS BIOTECH PRIVATE LIMITED

09 1Bills Biotech Private Limited

10 1Ceyone Life Sciences Private Limited

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PharmaCompass

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothWillow Birch Pharma delivers trusted, high-quality APIs nationwide with unmatched service, compliance, and competitive value.

ENCLOMIPHENE CITRATE

NDC Package Code : 10695-307

Start Marketing Date : 2025-04-01

End Marketing Date : 2026-12-31

Dosage Form (Strength) : POWDER (35kg/35kg)

Marketing Category : BULK INGREDIENT FOR HUMAN P...

Company Banner

05

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothWillow Birch Pharma delivers trusted, high-quality APIs nationwide with unmatched service, compliance, and competitive value.

ENCLOMIPHENE CITRATE

NDC Package Code : 10695-307

Start Marketing Date : 2025-05-07

End Marketing Date : 2026-12-31

Dosage Form (Strength) : POWDER (35kg/35kg)

Marketing Category : BULK INGREDIENT FOR HUMAN P...

Company Banner

06

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothWillow Birch Pharma delivers trusted, high-quality APIs nationwide with unmatched service, compliance, and competitive value.

ENCLOMIPHENE CITRATE

NDC Package Code : 10695-307

Start Marketing Date : 2025-05-07

End Marketing Date : 2026-12-31

Dosage Form (Strength) : POWDER (35kg/35kg)

Marketing Category : BULK INGREDIENT FOR HUMAN P...

Company Banner

07

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothWillow Birch Pharma delivers trusted, high-quality APIs nationwide with unmatched service, compliance, and competitive value.

ENCLOMIPHENE CITRATE

NDC Package Code : 10695-307

Start Marketing Date : 2025-04-01

End Marketing Date : 2026-12-31

Dosage Form (Strength) : POWDER (35kg/35kg)

Marketing Category : BULK INGREDIENT FOR HUMAN P...

Company Banner

08

Bioprocess International Europe
Not Confirmed
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Bioprocess International Europe
Not Confirmed

CLOMIPHENE CITRATE

NDC Package Code : 38779-0390

Start Marketing Date : 2014-07-31

End Marketing Date : 2026-12-31

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

Marketing Category : BULK INGREDIENT

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09

Bioprocess International Europe
Not Confirmed
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Bioprocess International Europe
Not Confirmed

CLOMIPHENE CITRATE

NDC Package Code : 17369-817

Start Marketing Date : 1982-01-01

End Marketing Date : 2026-12-31

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

Marketing Category : BULK INGREDIENT

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10

ASG Biochem Private Limited

Country
Bioprocess International Europe
Not Confirmed
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ASG Biochem Private Limited

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Bioprocess International Europe
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CLOMIPHENE CITRATE

NDC Package Code : 43647-136

Start Marketing Date : 2026-02-01

End Marketing Date : 2027-12-31

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

Marketing Category : BULK INGREDIENT

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Looking for 7619-53-6 / Clomiphene Citrate API manufacturers, exporters & distributors?

Clomiphene Citrate manufacturers, exporters & distributors 1

73

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

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

API | Excipient name

Clomiphene Citrate

Synonyms

50-41-9, Zuclomiphene citrate, Cis-clomiphene citrate, Clomid, Zuclomid, Clomiphene a citrate

Cas Number

7619-53-6

Unique Ingredient Identifier (UNII)

UY5X264QZV

About Clomiphene Citrate

A triphenyl ethylene stilbene derivative which is an estrogen agonist or antagonist depending on the target tissue. Note that ENCLOMIPHENE and ZUCLOMIPHENE are the (E) and (Z) isomers of Clomiphene respectively.

Clomid Manufacturers

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

Clomid Suppliers

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

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

Clomid 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 Clomid as an active pharmaceutical ingredient (API).

Finished drug products

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

click here to find a list of Clomid 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.