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List of all Manufacturers, Suppliers & Exporters of Tox21_300596 API listed on PharmaCompass with details of regulatory filings

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01 Biophore India Pharmaceuticals Pvt Ltd (2)

02 Transo-Pharm USA LLC (1)

03 Ahk Tech (1)

04 Aspen Biopharma Labs (1)

05 Axitec (1)

06 Cilag AG (2)

07 MSN Laboratories (2)

08 Mac-Chem Products (India) Pvt.Ltd (1)

09 Morepen Laboratories (1)

10 Reliable Biopharmaceutical Corporation (1)

11 ScinoPharm Taiwan, Ltd (1)

12 Shilpa Medicare (1)

13 Zhejiang Hisun Pharmaceutical (1)

14 Blank (1)

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01 China (3)

02 India (8)

03 Switzerland (2)

04 Taiwan (1)

05 U.S.A (2)

06 Blank (1)

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01 Active (9)

02 Inactive (3)

03 Blank (5)

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01 Valid (3)

02 Withdrawn by Holder (1)

03 Blank (13)

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01 305MF10067 (1)

02 Blank (16)

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01 WC-0349 (1)

02 Blank (16)

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USDMF

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CEP/COS

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Application Number
36221
Status
Active
Fees Paid
Reviewed
 
Filing Details
CLADRIBINE HPßCD COMPLEX
Issue/Submission Date
2021-08-30
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USDMF

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Issue/Submission Date
Transo Pharm USA Company Banner

Swiss Biotech Day

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USDMF

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Application Number
36222
Status
Active
Fees Paid
N/A
 
Filing Details
CLADRIBINE
Issue/Submission Date
2021-08-31
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USDMF

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Application Number
13006
Status
Active
Fees Paid
Reviewed
 
Filing Details
CLADRIBINE
Issue/Submission Date
1998-05-28
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USDMF

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Application Number
17603
Status
Active
Fees Paid
N/A
 
Filing Details
CLADRIBINE DRUG SUBSTANCE
Issue/Submission Date
2004-08-16
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USDMF

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Application Number
24510
R1-CEP 2016-315 - Rev 00
Status
Active
Fees Paid
Reviewed
Valid
 
Filing Details
CLADRIBINE USP
Cladribine
Issue/Submission Date
2010-12-30
2023-06-29
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USDMF

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Application Number
35806
R0-CEP 2021-217 - Rev 01
Indian CDSCO WC-0349
Status
Active
Fees Paid
N/A
Valid
 
Valid
2025-05-05
Filing Details
CLADRIBINE USP
Cladribine
Cladribine USP/Ph.Eur.
Issue/Submission Date
2021-03-31
2023-08-11
2022-09-02
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USDMF

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Application Number
36320
Status
Active
Fees Paid
Reviewed
 
Filing Details
CLADRIBINE CYCLODEXTRIN
Issue/Submission Date
2021-12-20
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USDMF

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Application Number
16205
R0-CEP 2012-132 - Rev 00
Status
Active
Fees Paid
Reviewed
Withdrawn by Holder
 
Filing Details
CLADRIBINE USP
Cladribine
Issue/Submission Date
2002-10-22
2014-10-29
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Application Number
23228
Status
Inactive
Fees Unpaid
N/A
 
Filing Details
CLADRIBINE NON-STERILE BULK DRUG
Issue/Submission Date
2009-10-16
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USDMF

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Application Number
12231
R0-CEP 2020-049 - Rev 00
305MF10067
Status
Inactive
Fees Paid
N/A
Valid
 
Filing Details
CLADRIBINE
Cladribine
Cladribine at Hochstrasse201 8200 S...
Issue/Submission Date
1996-11-21
2021-08-20
2023-05-24
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USDMF

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Application Number
18072
Status
Inactive
Fees Unpaid
N/A
 
Filing Details
CLADRIBINE
Issue/Submission Date
2005-01-31
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Application Number
31505
Status
Active
Fees Unpaid
N/A
 
Filing Details
CLADRIBINE DRUG SUBSTANCE
Issue/Submission Date
2017-05-05
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Looking for 4291-63-8 / Cladribine API manufacturers, exporters & distributors?

Cladribine manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Cladribine

Synonyms

2-chloro-2'-deoxyadenosine, 4291-63-8, Leustatin, 2-chlorodeoxyadenosine, 2-cda, Chlorodeoxyadenosine

Cas Number

4291-63-8

Unique Ingredient Identifier (UNII)

47M74X9YT5

About Cladribine

An antineoplastic agent used in the treatment of lymphoproliferative diseases including hairy-cell leukemia.

Tox21_300596 Manufacturers

A Tox21_300596 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_300596, including repackagers and relabelers. The FDA regulates Tox21_300596 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_300596 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 Tox21_300596 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Tox21_300596 Suppliers

A Tox21_300596 supplier is an individual or a company that provides Tox21_300596 active pharmaceutical ingredient (API) or Tox21_300596 finished formulations upon request. The Tox21_300596 suppliers may include Tox21_300596 API manufacturers, exporters, distributors and traders.

click here to find a list of Tox21_300596 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Tox21_300596 Manufacturers | Traders | Suppliers

Tox21_300596 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.
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