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List of NDC API details of PREVEN EMERGENCY CONTRACEPTIVE KIT Active Pharmaceutical Ingredient listed on PharmaCompass.com

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Flag India
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Ethinyl Estradiol
POWDER (1g/g)
BULK INGREDIENT
22552-0034
2012-06-27
2024-12-31
Flag Netherlands
Digital Content Digital Content
Ethinyl Estradiol
POWDER (1g/g)
BULK INGREDIENT
60870-0463
1980-04-25
2024-12-31
Flag India
Digital Content Digital Content
URL Supplier Web Content
Ethinyl Estradiol
POWDER (1kg/kg)
BULK INGREDIENT
43647-147
2023-08-10
2024-12-31
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Flag Germany
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Ethinylestradiol
POWDER (1kg/kg)
BULK INGREDIENT
12866-1016
2017-05-10
2024-12-31
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Ethinylestradiol
POWDER (1kg/kg)
BULK INGREDIENT
12866-1168
2017-05-10
2024-12-31
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Ethinyl Estradiol
POWDER (1kg/kg)
BULK INGREDIENT
65089-0044
2013-02-12
2024-12-31
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Ethinyl Estradiol
POWDER (1kg/kg)
BULK INGREDIENT
63190-0620
1982-01-01
2024-12-31
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Ethinylestradiol Micronized
POWDER (1kg/kg)
BULK INGREDIENT
63190-0740
2007-02-23
2024-12-31
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Ethinyl Estradiol
POWDER (1g/g)
BULK INGREDIENT
12860-0463
1980-04-25
2024-12-31
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ETHINYL ESTRADIOL
POWDER (1kg/kg)
BULK INGREDIENT FOR ...
51927-0305
2023-08-16
2024-12-31
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ETHINYL ESTRADIOL
POWDER (1kg/kg)
BULK INGREDIENT
44132-010
2014-06-17
2024-12-31
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ETHINYL ESTRADIOL
POWDER (1kg/kg)
BULK INGREDIENT
44132-002
2012-05-30
2024-12-31
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ethinylestradiol
POWDER (1kg/kg)
BULK INGREDIENT
60722-3017
2022-10-11
2024-12-31
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  • TABLET;ORAL-28 - 0.02MG;1MG
  • TABLET;ORAL-21 - 0.03MG;1.5MG
  • TABLET;ORAL-28 - 0.03MG;0.3MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • TABLET;ORAL-21 - 0.03MG;1.5MG
  • TABLET;ORAL-21 - 0.02MG;1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • TABLET;ORAL-28 - 0.035MG;1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • TABLET;ORAL-28 - 0.035MG,0.035MG,0.035MG;0.5MG,1MG,0.5MG
  • TABLET;ORAL-28 - 0.035MG,0.035MG,0.035MG;0.5MG,0.75MG,1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • TABLET;ORAL-28 - 0.035MG;0.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • TABLET;ORAL-28 - 0.035MG,0.035MG,0.035MG;0.18MG,0.215MG,0.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • TABLET;ORAL-21 - 0.02MG,0.03MG,0.035MG;1MG,1MG,1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • TABLET;ORAL-21 - 0.15MG;0.03MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • TABLET;ORAL - 0.02MG;1MG
  • TABLET;ORAL - 0.02MG,0.15MG;0.025MG,0.15MG;0.03MG,0.15MG;0.01MG,N/A
  • CAPSULE;ORAL - 0.02MG;1MG
  • TABLET, CHEWABLE, TABLET;ORAL - 0.01MG,0.01MG,N/A;1MG,N/A,N/A
  • TABLET;ORAL - 0.02MG;0.1MG
  • RING;VAGINAL - 0.013MG/24HR;0.15MG/24HR
  • TABLET;ORAL - 0.0025MG;0.5MG
  • TABLET;ORAL - 0.005MG;1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • TABLET;ORAL-28 - 0.1MG,0.125MG,0.15MG;0.025MG,0.025MG,0.025MG
  • FILM, EXTENDED RELEASE;TRANSDERMAL - 0.035MG/24HR;0.15MG/24HR **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • RING;VAGINAL - 0.015MG/24HR;0.12MG/24HR
  • TABLET;ORAL-28 - 0.025MG,0.025MG,0.025MG;0.18MG,0.215MG,0.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • TABLET;ORAL - 0.035MG;0.4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • TABLET;ORAL - 3MG;0.02MG
  • TABLET;ORAL - 0.02MG;1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • TABLET;ORAL - 0.01MG,0.01MG;1MG,N/A
  • TABLET, CHEWABLE;ORAL - 0.025MG;0.8MG

Looking for 57-63-6 / Ethinyl Estradiol API manufacturers, exporters & distributors?

Ethinyl Estradiol manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Ethinyl Estradiol

Synonyms

Ethynylestradiol, 57-63-6, Ethinylestradiol, Ethynyl estradiol, Ethinyloestradiol, 17-ethinylestradiol

Cas Number

57-63-6

Unique Ingredient Identifier (UNII)

423D2T571U

About Ethinyl Estradiol

A semisynthetic alkylated ESTRADIOL with a 17-alpha-ethinyl substitution. It has high estrogenic potency when administered orally, and is often used as the estrogenic component in ORAL CONTRACEPTIVES.

PREVEN EMERGENCY CONTRACEPTIVE KIT Manufacturers

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

PREVEN EMERGENCY CONTRACEPTIVE KIT Suppliers

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

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

PREVEN EMERGENCY CONTRACEPTIVE KIT 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 PREVEN EMERGENCY CONTRACEPTIVE KIT as an active pharmaceutical ingredient (API).

Finished drug products

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

click here to find a list of PREVEN EMERGENCY CONTRACEPTIVE KIT suppliers with NDC on PharmaCompass.

PREVEN EMERGENCY CONTRACEPTIVE KIT Manufacturers | Traders | Suppliers

PREVEN EMERGENCY CONTRACEPTIVE KIT Manufacturers, Traders, Suppliers 1
69

We have 10 companies offering PREVEN EMERGENCY CONTRACEPTIVE KIT

Get in contact with the supplier of your choice:

  1. Aspen API
  2. Symbiotec Pharmalab
  3. ASG Biochem
  4. Bayer AG
  5. Curia
  6. Industriale Chimica s.r.l.
  7. Merck & Co
  8. Pcca
  9. Qinhuangdao Zizhu Pharmaceutical Co., Ltd.
  10. Zhejiang Xianju Pharmaceutical Co. Ltd
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.
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