Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
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01 1Biophore India Pharmaceuticals Pvt Ltd
02 1LGM Pharma
03 1AASraw Biochemical Technology Co., Ltd
04 1Asia Pioneer Pharmaceuticals
05 1BASF
06 1Catalent Pharma Solutions
07 2Chongqing Huapont Pharmaceutical
08 1EASTMAN KODAK
09 1F. Hoffmann-La Roche
10 1HAS Healthcare Advanced Synthesis
11 1Hangzhou Deli Chemical
12 1Helsinn Advanced Synthesis
13 1Hetero Drugs
14 1Ipca Laboratories
15 1JIANGXI HENGXIANG PHARMACEUTICAL TECHNOLOGY CO LTD
16 1Kimia Biosciences
17 1Kukjeon Pharmaceutical
18 1Nishchem International Pvt. Ltd
19 2Olon S.p.A
20 1Qingdao Qingmei Biotech
21 1RP SCHERER GMBH & CO. KG
22 1SAMEX OVERSEAS
23 1Shanghai New Hualian Pharmaceutical
24 1Shanghai Pharma Group
25 1Siegfried AG
26 1Sionc Pharmaceuticals
27 3Sun Pharmaceutical Industries Limited
28 1Unipex
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01 8China
02 1France
03 2Germany
04 10India
05 2Italy
06 1South Korea
07 4Switzerland
08 4U.S.A
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01 9Active
02 6Inactive
03 17Blank
01 8Valid
02 2Withdrawn by Holder
03 22Blank
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01 32Blank
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01 1WC-0011nA2
02 1WC-0159
03 1WC-0168
04 29Blank
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01 120171226-209-J-4
02 120180712-209-J-72
03 120190327-209-J-207
04 29Blank
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01 117337-0024
02 117337-0083
03 148943-0010
04 165724-0051
05 165977-0135
06 167262-0003
07 176055-0010
08 25Blank
01 32Blank
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
GDUFA
DMF Review : Reviewed
Rev. Date : 2014-05-13
Pay. Date : 2013-09-25
DMF Number : 27484
Submission : 2013-09-27
Status : Active
Type : II
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-01-14
Pay. Date : 2012-12-10
DMF Number : 7485
Submission : 1988-05-16
Status : Active
Type : II
Certificate Number : R1-CEP 1996-082 - Rev 12
Issue Date : 2022-04-12
Type : Chemical
Substance Number : 1019
Status : Valid
NDC Package Code : 17337-0083
Start Marketing Date : 2017-09-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19191
Submission : 2005-10-25
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2017-09-28
Pay. Date : 2016-09-30
DMF Number : 21653
Submission : 2008-05-23
Status : Active
Type : II
Certificate Number : CEP 2018-219 - Rev 01
Issue Date : 2023-12-06
Type : Chemical
Substance Number : 1019
Status : Valid
NDC Package Code : 48943-0010
Start Marketing Date : 2003-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Ace Biopharm Co., Ltd.
Registration Date : 2017-12-26
Registration Number : 20171226-209-J-4
Manufacturer Name : Chongqing Huapont Shengchem Pharmaceutical Co., Ltd.
Manufacturer Address : No. 666 Rongjun Road, Nanjin Avenue Hechuan District, Chongqing China
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 34510
Submission : 2020-02-12
Status : Active
Type : II
Certificate Number : R1-CEP 2009-330 - Rev 00
Issue Date : 2016-10-13
Type : Chemical
Substance Number : 1019
Status : Valid
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-05-09
Pay. Date : 2012-12-14
DMF Number : 19918
Submission : 2006-10-30
Status : Active
Type : II
Certificate Number : R1-CEP 2004-281 - Rev 01
Issue Date : 2022-03-01
Type : Chemical
Substance Number : 1019
Status : Valid
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13071
Submission : 1998-07-01
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14493
Submission : 1999-10-14
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4887
Submission : 1983-03-23
Status : Inactive
Type : II
17
PharmaCompass offers a list of Isotretinoin 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 Isotretinoin manufacturer or Isotretinoin supplier for your needs.
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A isotretinoina manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of isotretinoina, including repackagers and relabelers. The FDA regulates isotretinoina manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. isotretinoina API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A isotretinoina supplier is an individual or a company that provides isotretinoina active pharmaceutical ingredient (API) or isotretinoina finished formulations upon request. The isotretinoina suppliers may include isotretinoina API manufacturers, exporters, distributors and traders.
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We have 28 companies offering isotretinoina
Get in contact with the supplier of your choice: