Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
01 1Biophore India Pharmaceuticals Pvt Ltd
02 1LGM Pharma
03 1Jai Radhe Sales
04 1Amcol
05 1BASF
06 1Catalent Pharma Solutions
07 1Chongqing Huapont Pharmaceutical
08 1Cilag AG
09 1EASTMAN KODAK
10 1F. Hoffmann-La Roche
11 1Hangzhou Deli Chemical
12 1Hangzhou Think Chemical Co.Ltd
13 1Kawaken Fine Chemicals
14 1Northeast Pharmaceutical Group Co Ltd
15 2Olon S.p.A
16 1RANBAXY LABORATORIES LIMITED
17 1SAMEX OVERSEAS
18 1Siegfried AG
19 1Sionc Pharmaceuticals
20 1Srikem Laboratories Pvt. Ltd
21 1Tecoland Corporation
22 1Blank
01 4China
02 1Germany
03 6India
04 2Italy
05 1Japan
06 3Switzerland
07 5U.S.A
08 1Blank
01 6Active
02 7Inactive
03 10Blank
01 5Valid
02 18Blank
01 1219MF10174
02 1229MF10001
03 21Blank
01 1WC-0273
02 22Blank
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-09-03
Pay. Date : 2013-03-19
DMF Number : 26922
Submission : 2013-03-30
Status : Active
Type : II
Certificate Number : R0-CEP 2019-124 - Rev 00
Issue Date : 2021-07-01
Type : Chemical
Substance Number : 693
Status : Valid
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
GDUFA
DMF Review : Reviewed
Rev. Date : 2019-10-02
Pay. Date : 2019-09-25
DMF Number : 7474
Submission : 1988-05-11
Status : Active
Type : II
Certificate Number : R1-CEP 1998-082 - Rev 07
Issue Date : 2021-06-18
Type : Chemical
Substance Number : 693
Status : Valid
Registration Number : 229MF10001
Registrant's Address : Strada Rivoltana, km 6/7, 20053 Rodano (MI), Italy
Initial Date of Registration : 2017-01-10
Latest Date of Registration :
NDC Package Code : 17337-0036
Start Marketing Date : 2012-12-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : DKS Korea Co., Ltd.
Registration Date : 2022-12-05
Registration Number : 20221205-209-J-1392
Manufacturer Name : Olon SPA
Manufacturer Address : Via Milano 186 I-20024 Garbagnate Milanese Milano, Italy
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 25192
Submission : 2011-08-03
Status : Active
Type : II
Certificate Number : R1-CEP 2010-034 - Rev 01
Issue Date : 2021-07-02
Type : Chemical
Substance Number : 693
Status : Valid
NDC Package Code : 17337-0036
Start Marketing Date : 2012-12-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : DKS Korea Co., Ltd.
Registration Date : 2022-12-05
Registration Number : 20221205-209-J-1392
Manufacturer Name : Olon SPA
Manufacturer Address : Via Milano 186 I-20024 Garbagnate Milanese Milano, Italy
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-09-04
Pay. Date : 2013-08-27
DMF Number : 3456
Submission : 1978-12-21
Status : Active
Type : II
Certificate Number : R1-CEP 2009-350 - Rev 01
Issue Date : 2016-04-22
Type : Chemical
Substance Number : 693
Status : Valid
NDC Package Code : 65724-0052
Start Marketing Date : 2010-06-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : CTC Bio Co., Ltd.
Registration Date : 2022-09-26
Registration Number : 20220926-209-J-1368
Manufacturer Name : Siegfried PharmaChemikalien Minden GmbH
Manufacturer Address : Karlstraße 15-39, 42-44 32423 Minden, Germany
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 27398
Submission : 2013-07-30
Status : Active
Type : II
Certificate Number : R0-CEP 2020-183 - Rev 00
Issue Date : 2022-09-05
Type : Chemical
Substance Number : 693
Status : Valid
NDC Package Code : 48943-0011
Start Marketing Date : 2000-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Ace Biopharm Co., Ltd.
Registration Date : 2021-10-21
Registration Number : 20211021-209-J-1068
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 : 23186
Submission : 2009-10-15
Status : Active
Type : II
NDC Package Code : 68634-069
Start Marketing Date : 2017-01-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (10g/kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4463
Submission : 1982-02-24
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 1192
Submission : 1968-06-03
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 24420
Submission : 2010-12-07
Status : Inactive
Type : II
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7996
Submission : 1989-04-04
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11580
Submission : 1995-07-13
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10972
Submission : 1994-06-28
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8592
Submission : 1990-06-08
Status : Inactive
Type : II
Date of Issue : 2020-07-23
Valid Till : 2023-05-11
Written Confirmation Number : WC-0273
Address of the Firm :
NDC Package Code : 76055-0007
Start Marketing Date : 2019-12-31
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registration Number : 219MF10174
Registrant's Address : 2-3-3 Nihonbashi Horidomecho, Chuo-ku, Tokyo
Initial Date of Registration : 2007-06-01
Latest Date of Registration :
A Tretinoin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tretinoin, including repackagers and relabelers. The FDA regulates Tretinoin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tretinoin 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 Tretinoin supplier is an individual or a company that provides Tretinoin active pharmaceutical ingredient (API) or Tretinoin finished formulations upon request. The Tretinoin suppliers may include Tretinoin API manufacturers, exporters, distributors and traders.
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