Octavius has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
01 1Octavius Pharma Pvt. Ltd
02 1Bayer AG
03 1CKD Bio Corporation
04 2CSPC Pharmaceutical Group
05 1HAUDONG MEDICINE CO LTD
06 1Hangzhou Zhongmei Huadong Pharmaceutical
07 1Livzon Group Fuzhou Fuxing Pharmaceutical Co., Ltd.
08 1Livzon New North River Pharmaceutical
09 1Qingdao Qingmei Biotech
10 1Tecoland Corporation
11 1Tocopharm Co. Limited
12 1Zhejiang Hisun Pharmaceutical
01 9China
02 1Germany
03 1India
04 1South Korea
05 1U.S.A
01 8Active
02 1Inactive
03 4Blank
01 6Valid
02 7Blank
01 1218MF10411
02 1220MF10038
03 1303MF10047
04 10Blank
01 13Blank
Octavius has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 25207
Submission : 2011-07-11
Status : Active
Type : II
Certificate Number : R1-CEP 2011-054 - Rev 03
Issue Date : 2020-03-05
Type : Chemical
Substance Number : 2089
Status : Valid
Registration Number : 303MF10047
Registrant's Address : No. 48 Shengxue Road, Luncheng District, Shijiazhuang City, Hebei Province, China
Initial Date of Registration : 2021-03-17
Latest Date of Registration : --
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 35603
Submission : 2021-03-01
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8539
Submission : 1990-04-23
Status : Active
Type : II
Certificate Number : R1-CEP 2007-101 - Rev 03
Issue Date : 2018-03-06
Type : Chemical
Substance Number : 2089
Status : Valid
Registrant Name : Bayer Korea Ltd.
Registration Date : 2013-01-04
Registration Number : 20130104-153-I-168-01
Manufacturer Name : Bayer AG
Manufacturer Address : Friedrich-Ebert-Str. 217-333, D-42117 Wuppertal
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-03-15
Pay. Date : 2013-02-26
DMF Number : 20759
Submission : 2007-07-31
Status : Active
Type : II
Certificate Number : R1-CEP 2007-252 - Rev 02
Issue Date : 2017-01-27
Type : Chemical
Substance Number : 2089
Status : Valid
Registration Number : 220MF10038
Registrant's Address : 8, Chungjeong-ro, Seodaemun-gu, Seoul, Republic of Korea
Initial Date of Registration : 2008-02-05
Latest Date of Registration : --
NDC Package Code : 52972-0035
Start Marketing Date : 2007-09-12
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Chong Kun Dang Bio Co., Ltd.
Registration Date : 2013-04-03
Registration Number : 20130403-153-I-293-02
Manufacturer Name : Chong Kun Dang Bio Co., Ltd.
Manufacturer Address : (425-100) 292 Sinwon-ro, Danwon-gu, Ansan-si, Gyeonggi-do
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 37145
Submission : 2022-07-20
Status : Active
Type : II
Certificate Number : CEP 2009-224 - Rev 05
Issue Date : 2024-06-12
Type : Chemical
Substance Number : 2089
Status : Valid
NDC Package Code : 65897-4005
Start Marketing Date : 2022-12-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-09-22
Pay. Date : 2013-04-11
DMF Number : 18138
Submission : 2005-02-24
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2021-06-07
Pay. Date : 2021-03-17
DMF Number : 35188
Submission : 2020-10-30
Status : Active
Type : II
Certificate Number : R0-CEP 2021-063 - Rev 01
Issue Date : 2022-04-01
Type : Chemical
Substance Number : 2089
Status : Valid
NDC Package Code : 42513-0016
Start Marketing Date : 2021-01-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2012-11-23
Pay. Date : 2012-11-15
DMF Number : 19069
Submission : 2005-12-14
Status : Active
Type : II
Certificate Number : R1-CEP 2006-144 - Rev 01
Issue Date : 2021-03-17
Type : Chemical
Substance Number : 2089
Status : Valid
Registration Number : 218MF10411
Registrant's Address : 46 Waisha Road, Jiaojiang District, Taizhou City, Zhejiang Province, P. R. China 318000
Initial Date of Registration : 2006-04-14
Latest Date of Registration : --
NDC Package Code : 58623-0022
Start Marketing Date : 2008-05-07
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 : 23279
Submission : 2009-11-18
Status : Inactive
Type : II
A Acarbose manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Acarbose, including repackagers and relabelers. The FDA regulates Acarbose manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Acarbose 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 Acarbose manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Acarbose supplier is an individual or a company that provides Acarbose active pharmaceutical ingredient (API) or Acarbose finished formulations upon request. The Acarbose suppliers may include Acarbose API manufacturers, exporters, distributors and traders.
click here to find a list of Acarbose suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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