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01 1Hubei Gedian Humanwell Pharmaceutical Co., Ltd

02 3Industriale Chimica s.r.l.

03 2NEWCHEM SPA

04 1Quimica Sintetica S.A.

05 2STERLING SPA

06 1SYMBIOTICA SPECIALITY INGREDIENTS SDN.BHD

07 1Sicor S.r.l.

08 2Sterling Chemical Malta Ltd

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PharmaCompass

02

The Generic Rx Session
Not Confirmed
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DROSPIRENONE

NDC Package Code : 63190-0240

Start Marketing Date : 2007-07-11

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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03

The Generic Rx Session
Not Confirmed
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The Generic Rx Session
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DROSPIRENONE

NDC Package Code : 63190-0230

Start Marketing Date : 2007-07-11

End Marketing Date : 2025-12-31

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

DROSPIRENONE

NDC Package Code : 24002-0002

Start Marketing Date : 2009-08-10

End Marketing Date : 2024-12-31

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

Marketing Category : BULK INGREDIENT

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05

The Generic Rx Session
Not Confirmed
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The Generic Rx Session
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DROSPIRENONE

NDC Package Code : 24002-0037

Start Marketing Date : 2021-12-01

End Marketing Date : 2024-12-31

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
Not Confirmed

DROSPIRENONE

NDC Package Code : 53069-0990

Start Marketing Date : 2001-05-11

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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DROSPIRENONE

NDC Package Code : 53183-9037

Start Marketing Date : 2017-02-15

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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08

The Generic Rx Session
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DROSPIRENONE

NDC Package Code : 59057-015

Start Marketing Date : 2023-05-12

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
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The Generic Rx Session
Not Confirmed

DROSPIRENONE

NDC Package Code : 59057-014

Start Marketing Date : 2023-05-12

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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Looking for 67392-87-4 / Drospirenone API manufacturers, exporters & distributors?

Drospirenone manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Drospirenone

Synonyms

67392-87-4, Dihydrospirorenone, Dehydrospirorenone, Drospirenona, 1,2-dihydrospirorenone, Drsp

Cas Number

67392-87-4

Unique Ingredient Identifier (UNII)

N295J34A25

About Drospirenone

Drospirenone is a synthetic spironolactone analogue and progestin with progestational and anti-mineralocorticoid activity. Drospirenone binds to the progesterone receptor, the resulting complex becomes activated and binds to specific sites on DNA. This results in a suppression of LH activity and an inhibition of ovulation as well as an alteration in the cervical mucus and endometrium. This leads to an increased difficulty of sperm entry into the uterus and implantation. This drug is used in oral contraceptives.

Drospirenone Manufacturers

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

Drospirenone Suppliers

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

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

Drospirenone 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 Drospirenone as an active pharmaceutical ingredient (API).

Finished drug products

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

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

Drospirenone Manufacturers | Traders | Suppliers

Drospirenone 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.