Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
01 2Aarti Pharmalabs
02 1American Pacific Corporation
03 1Apicore LLC
04 2Apothecon Pharmaceuticals
05 1BEDFORD LABS
06 2Baxter Healthcare Corporation
07 2Emcure Pharmaceuticals
08 1Hetero Drugs
09 1Jiangsu Hengrui Medicine
10 1LIANYUNGANG GUIKE PHARMACEUTICAL
11 1MSN Laboratories
12 1POLYPHARMA TECH & SCIENCES
13 1Shilpa Medicare
14 2Sunny Pharmtech
15 1Zhejiang Hisun Pharmaceutical
16 1Blank
01 3CYCLOPHOSPHAMIDE
02 1CYCLOPHOSPHAMIDE INJECTION VIALS
03 1CYCLOPHOSPHAMIDE LYOPHILIZED FOR INJ(5 DOSAGE FORMS)BEDFORD,OHIO FAC
04 1CYCLOPHOSPHAMIDE MONOHYDRATE
05 1CYCLOPHOSPHAMIDE MONOHYDRATE USP
06 1CYCLOPHOSPHAMIDE MONOHYDRATE, USP
07 1CYCLOPHOSPHAMIDE STERILE USP
08 7CYCLOPHOSPHAMIDE USP
09 1CYCLOPHOSPHAMIDE USP (STERILE BULK)
10 1CYCLOPHOSPHAMIDE USP (STERILE)
11 1CYCLOPHOSPHAMIDE USP,NON-STERILE BULK DRUG
12 1CYCLOPHOSPHAMIDE, USP, STERILE, BULK DRUG SUBSTANCE
13 1CYCLOPHOSPHAMIDE, USP/EP
01 3China
02 1Germany
03 10India
04 2Taiwan
05 4U.S.A
06 1Blank
01 16Active
02 5Inactive
01 9Complete
02 12Blank
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 35313
Submission : 2021-01-21
Status : Active
Type : II
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 37086
Submission : 2022-05-02
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 32492
Submission : 2018-02-09
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3716
Submission : 1980-01-29
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3594
Submission : 1979-06-11
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2015-12-15
Pay. Date : 2015-09-29
DMF Number : 29839
Submission : 2015-09-30
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2015-04-15
Pay. Date : 2015-03-20
DMF Number : 26753
Submission : 2012-12-21
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 26041
Submission : 2012-05-11
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2017-06-08
Pay. Date : 2017-05-22
DMF Number : 31088
Submission : 2016-12-01
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-01-18
Pay. Date : 2012-12-18
DMF Number : 15178
Submission : 2000-12-01
Status : Active
Type : II
A Cyclophosphamide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cyclophosphamide, including repackagers and relabelers. The FDA regulates Cyclophosphamide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cyclophosphamide 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 Cyclophosphamide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cyclophosphamide supplier is an individual or a company that provides Cyclophosphamide active pharmaceutical ingredient (API) or Cyclophosphamide finished formulations upon request. The Cyclophosphamide suppliers may include Cyclophosphamide API manufacturers, exporters, distributors and traders.
click here to find a list of Cyclophosphamide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cyclophosphamide DMF (Drug Master File) is a document detailing the whole manufacturing process of Cyclophosphamide active pharmaceutical ingredient (API) in detail. Different forms of Cyclophosphamide DMFs exist exist since differing nations have different regulations, such as Cyclophosphamide USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Cyclophosphamide DMF submitted to regulatory agencies in the US is known as a USDMF. Cyclophosphamide USDMF includes data on Cyclophosphamide's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Cyclophosphamide USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Cyclophosphamide suppliers with USDMF on PharmaCompass.
We have 15 companies offering Cyclophosphamide
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?