Century has been an API manufacturer for over 30 years & is the partner of choice for multipurpose custom manufacturing projects.
01 1Century Pharmaceuticals
02 1Fermic
03 1HUASHU PHARMACEUTICAL CORPORATION
04 1IBI Spa
05 1Krka
06 1Mitsubishi Corporation
07 5Pfizer Inc
08 1Pliva Hrvatska
09 1Sichuan Long March Pharmaceutical Co. Ltd.
10 3Blank
01 13OXYTETRACYCLINE
02 1OXYTETRACYCLINE BASE
03 1OXYTETRACYCLINE DIHYDRATE
04 1OXYTETRACYCLINE DIHYDRATE USP
01 2China
02 1Croatia
03 1India
04 1Italy
05 1Japan
06 1Mexico
07 1Slovenia
08 5U.S.A
09 3Blank
01 2Active
02 14Inactive
01 16Blank
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
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 : 11650
Submission : 1995-09-08
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13305
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 : 13451
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 : 13302
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 : 13350
Submission : 1998-09-01
Status : Inactive
Type : II
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.
A Oxytetracycline Dihydrate DMF (Drug Master File) is a document detailing the whole manufacturing process of Oxytetracycline Dihydrate active pharmaceutical ingredient (API) in detail. Different forms of Oxytetracycline Dihydrate DMFs exist exist since differing nations have different regulations, such as Oxytetracycline Dihydrate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Oxytetracycline Dihydrate DMF submitted to regulatory agencies in the US is known as a USDMF. Oxytetracycline Dihydrate USDMF includes data on Oxytetracycline Dihydrate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Oxytetracycline Dihydrate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Oxytetracycline Dihydrate suppliers with USDMF on PharmaCompass.
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