SCI Pharmtech offers high-quality, cost-effective APIs, advanced intermediates, & custom products with global expertise and precision.
01 1SCI Pharmtech
02 1ACE Japan Co Ltd
03 1Catalytica
04 1Sumitomo Chemical
05 1Zambon Switzerland
06 2Blank
01 1India
02 2Japan
03 1Switzerland
04 1Taiwan
05 2Blank
01 1Active
02 4Inactive
03 2Blank
01 7Blank
01 1222MF10231
02 1229MF10022
03 1305MF10113
04 4Blank
01 7Blank
SCI Pharmtech offers high-quality, cost-effective APIs, advanced intermediates, & custom products with global expertise and precision.
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GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17355
Submission : 2004-04-26
Status : Active
Type : II
Registration Number : 229MF10022
Registrant's Address : No. 61, Ln. 309, Haihu N. Rd. , Luzhu Dist. , Taoyuan City 33856, Taiwan
Initial Date of Registration : 2017-01-31
Latest Date of Registration :
NDC Package Code : 68108-0304
Start Marketing Date : 2004-06-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
| Available Reg Filing : CA |
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 : 2167
Submission : 1973-10-17
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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 : 7761
Submission : 1988-11-22
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 : 8286
Submission : 1989-11-14
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8258
Submission : 1989-10-20
Status : Inactive
Type : II
Registration Number : 305MF10113
Registrant's Address : Yamagata Prefecture Higashine City Higashine City 5850-1
Initial Date of Registration : 2023-10-04
Latest Date of Registration :
Registration Number : 222MF10231
Registrant's Address : 2-27-1 Shinkawa, Chuo-ku, Tokyo
Initial Date of Registration : 2010-09-24
Latest Date of Registration :
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A Probucol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Probucol, including repackagers and relabelers. The FDA regulates Probucol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Probucol 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 Probucol supplier is an individual or a company that provides Probucol active pharmaceutical ingredient (API) or Probucol finished formulations upon request. The Probucol suppliers may include Probucol API manufacturers, exporters, distributors and traders.
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We have 5 companies offering Probucol
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