Suanfarma, at the Core of a Better Life.
01 1Suanfarma
02 1Century Pharmaceuticals
03 1BOC Sciences
04 1Fermic
05 1Grand Health Industrial Co Ltd
06 2HEBEI JIANMIN STARCH GLUCOSE CO, LTD
07 1HUASHU PHARMACEUTICAL CORPORATION
08 1Hangzhou Think Chemical Co.Ltd
09 3Hebei Shengxue Dacheng Pharmaceutical Co
10 1Hebei Veyong Pharmaceutical
11 1IBI Spa
12 1Inner Mongolia Changsheng Pharmaceutical
13 2Krka
14 1Mitsubishi Corporation
15 1Norbrook Laboratories
16 5Pfizer Inc
17 1Pliva Hrvatska
18 1SHANDONG JINYANG PHARMACEUTICAL CO., LTD. CN 255000 Zibo City
19 2Shanghai Hegno Pharmaceutical
20 1Sichuan Long March Pharmaceutical Co. Ltd.
21 3Yangzhou Liberty Pharmaceutical
22 3Blank
01 17China
02 1Croatia
03 1India
04 1Italy
05 1Japan
06 1Mexico
07 2Slovenia
08 1Spain
09 6U.S.A
10 1United Kingdom
11 3Blank
01 2Active
02 14Inactive
03 19Blank
01 10Valid
02 3Withdrawn by EDQM Failure to CEP procedure
03 3Withdrawn by Holder
04 19Blank
01 35Blank
01 1WC-0293
02 34Blank
Century has been an API manufacturer for over 30 years & is the partner of choice for multipurpose custom manufacturing projects.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 34584
Submission : 2020-03-13
Status : Active
Type : II
Date of Issue : 2022-11-02
Valid Till : 2024-12-16
Written Confirmation Number : WC-0293
Address of the Firm :
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11650
Submission : 1995-09-08
Status : Active
Type : II
Certificate Number : R1-CEP 2002-211 - Rev 00
Issue Date : 2012-10-26
Type : Chemical
Substance Number : 199
Status : Withdrawn by EDQM F...
VMF Number : 5674
Submission : 1999-12-06
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13641
Submission : 1998-09-01
Status : Inactive
Type : II
NDC Package Code : 51671-0002
Start Marketing Date : 2010-12-17
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13302
Submission : 1998-09-01
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13322
Submission : 1998-09-01
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13451
Submission : 1998-09-01
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13472
Submission : 1998-09-01
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13488
Submission : 1998-09-01
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13507
Submission : 1998-09-01
Status : Inactive
Type : II
Certificate Number : R0-CEP 2003-274 - Rev 00
Issue Date : 2005-09-30
Type : Chemical
Substance Number : 199
Status : Withdrawn by Holder
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13350
Submission : 1998-09-01
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13367
Submission : 1998-09-01
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13463
Submission : 1998-09-01
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13305
Submission : 1998-09-01
Status : Inactive
Type : II
Certificate Number : R1-CEP 2011-079 - Rev 01
Issue Date : 2017-05-24
Type : Chemical
Substance Number : 199
Status : Withdrawn by EDQM F...
NDC Package Code : 54509-0001
Start Marketing Date : 2013-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
VMF Number : 6023
Submission : 2012-09-11
Status : Active
Type : II
Certificate Number : R0-CEP 2018-238 - Rev 00
Issue Date : 2020-01-17
Type : Chemical
Substance Number : 199
Status : Valid
NDC Package Code : 70831-101
Start Marketing Date : 2016-07-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Certificate Number : R1-CEP 2002-035 - Rev 03
Issue Date : 2023-03-13
Type : Chemical
Substance Number : 199
Status : Valid
NDC Package Code : 60264-110
Start Marketing Date : 2003-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
VMF Number : 5744
Submission : 2002-05-29
Status : Active
Type : II
Certificate Number : R1-CEP 2009-053 - Rev 02
Issue Date : 2023-03-13
Type : Chemical
Substance Number : 199
Status : Valid
NDC Package Code : 60264-110
Start Marketing Date : 2003-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
VMF Number : 5744
Submission : 2002-05-29
Status : Active
Type : II
Certificate Number : CEP 2004-055 - Rev 03
Issue Date : 2024-10-09
Type : Chemical
Substance Number : 199
Status : Valid
NDC Package Code : 24507-001
Start Marketing Date : 2011-01-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
VMF Number : 6073
Submission : 2014-06-03
Status : Active
Type : II
Certificate Number : R0-CEP 2021-031 - Rev 00
Issue Date : 2022-06-23
Type : Chemical
Substance Number : 199
Status : Valid
NDC Package Code : 24507-001
Start Marketing Date : 2011-01-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
VMF Number : 6073
Submission : 2014-06-03
Status : Active
Type : II
Certificate Number : CEP 2018-291 - Rev 01
Issue Date : 2024-08-30
Type : Chemical
Substance Number : 199
Status : Valid
VMF Number : 6101
Submission : 2019-09-11
Status : Active
Type : II
Certificate Number : R1-CEP 1999-133 - Rev 01
Issue Date : 2007-07-31
Type : Chemical
Substance Number : 199
Status : Withdrawn by Holder
Certificate Number : CEP 2017-258 - Rev 01
Issue Date : 2024-05-22
Type : Chemical
Substance Number : 199
Status : Valid
NDC Package Code : 24507-001
Start Marketing Date : 2011-01-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
VMF Number : 6073
Submission : 2014-06-03
Status : Active
Type : II
Certificate Number : R1-CEP 1997-127 - Rev 06
Issue Date : 2017-04-19
Type : Chemical
Substance Number : 199
Status : Valid
Certificate Number : R0-CEP 2004-177 - Rev 00
Issue Date : 2007-11-15
Type : Chemical
Substance Number : 199
Status : Withdrawn by Holder
Certificate Number : R1-CEP 2017-105 - Rev 00
Issue Date : 2023-03-15
Type : Chemical
Substance Number : 199
Status : Valid
VMF Number : 6101
Submission : 2019-09-11
Status : Active
Type : II
Certificate Number : R0-CEP 2023-054 - Rev 00
Issue Date : 2023-05-26
Type : Chemical
Substance Number : 199
Status : Valid
VMF Number : 6101
Submission : 2019-09-11
Status : Active
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 : 13573
Submission : 1998-09-01
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 : 13672
Submission : 1998-09-01
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 : 13766
Submission : 1998-09-01
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
A Oxytetracycline Dihydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxytetracycline Dihydrate, including repackagers and relabelers. The FDA regulates Oxytetracycline Dihydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxytetracycline Dihydrate 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 Oxytetracycline Dihydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Oxytetracycline Dihydrate supplier is an individual or a company that provides Oxytetracycline Dihydrate active pharmaceutical ingredient (API) or Oxytetracycline Dihydrate finished formulations upon request. The Oxytetracycline Dihydrate suppliers may include Oxytetracycline Dihydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Oxytetracycline Dihydrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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