Aarti Pharmalabs is a partner of choice for pharmaceutical companies for APIs & Intermediates. Largest Indian producer of Caffeine.

Reset all filters
01 2Aarti Pharmalabs
02 1American Pacific Corporation
03 1Apicore
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
Reset all filters
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
Reset all filters
01 3China
02 1Germany
03 10India
04 2Taiwan
05 4U.S.A
06 1Blank
Reset all filters
01 16Active
02 5Inactive
Reset all filters
01 9Complete
02 12Blank
Aarti Pharmalabs is a partner of choice for pharmaceutical companies for APIs & Intermediates. Largest Indian producer of Caffeine.
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 pharmaceutical companies for APIs & Intermediates. Largest Indian producer of Caffeine.
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

33
PharmaCompass offers a list of Cyclophosphamide 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 Cyclophosphamide manufacturer or Cyclophosphamide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cyclophosphamide manufacturer or Cyclophosphamide supplier.
PharmaCompass also assists you with knowing the Cyclophosphamide API Price utilized in the formulation of products. Cyclophosphamide API Price is not always fixed or binding as the Cyclophosphamide Price is obtained through a variety of data sources. The Cyclophosphamide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A C07888 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of C07888, including repackagers and relabelers. The FDA regulates C07888 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. C07888 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 C07888 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A C07888 supplier is an individual or a company that provides C07888 active pharmaceutical ingredient (API) or C07888 finished formulations upon request. The C07888 suppliers may include C07888 API manufacturers, exporters, distributors and traders.
click here to find a list of C07888 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A C07888 DMF (Drug Master File) is a document detailing the whole manufacturing process of C07888 active pharmaceutical ingredient (API) in detail. Different forms of C07888 DMFs exist exist since differing nations have different regulations, such as C07888 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A C07888 DMF submitted to regulatory agencies in the US is known as a USDMF. C07888 USDMF includes data on C07888's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The C07888 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of C07888 suppliers with USDMF on PharmaCompass.
We have 15 companies offering C07888
Get in contact with the supplier of your choice: