01 1Actavis Inc
02 2Changzhou Pharmaceutical Factory
03 1HUASHU PHARMACEUTICAL CORPORATION
04 2Hovione
05 1KUNSHAN ORIENTAL PHARMACEUTICAL CO LTD
06 1RANBAXY LABORATORIES LIMITED
07 1Raks Pharma
08 1Yangzhou Pharmaceutical
09 1Blank
01 3DOXYCYCLINE
02 1DOXYCYCLINE (ROUTE CODE: DX)
03 3DOXYCYCLINE MONOHYDRATE
04 1DOXYCYCLINE MONOHYDRATE MICRONIZED
05 2DOXYCYCLINE USP
06 1DOXYCYCLINE USP, NON-STERILE BULK DRUG
01 5China
02 2India
03 1Ireland
04 2Portugal
05 1Blank
01 6Active
02 5Inactive
01 5Complete
02 6Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13500
Submission : 1998-09-01
Status : Inactive
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2014-05-26
Pay. Date : 2014-05-14
DMF Number : 18959
Submission : 2005-11-09
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2024-04-16
Pay. Date : 2024-04-02
DMF Number : 39292
Submission : 2023-12-22
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-01-09
Pay. Date : 2012-12-11
DMF Number : 23638
Submission : 2010-03-18
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-01-11
Pay. Date : 2012-12-11
DMF Number : 13710
Submission : 1998-09-01
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13040
Submission : 1998-06-25
Status : Inactive
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2021-08-10
Pay. Date : 2021-08-06
DMF Number : 25062
Submission : 2011-06-16
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14295
Submission : 1999-07-14
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13944
Submission : 1999-01-13
Status : Active
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13450
Submission : 1998-09-01
Status : Inactive
Type : II
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A Doxycycline (anhydrous) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Doxycycline (anhydrous), including repackagers and relabelers. The FDA regulates Doxycycline (anhydrous) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Doxycycline (anhydrous) 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 Doxycycline (anhydrous) manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Doxycycline (anhydrous) supplier is an individual or a company that provides Doxycycline (anhydrous) active pharmaceutical ingredient (API) or Doxycycline (anhydrous) finished formulations upon request. The Doxycycline (anhydrous) suppliers may include Doxycycline (anhydrous) API manufacturers, exporters, distributors and traders.
click here to find a list of Doxycycline (anhydrous) suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Doxycycline (anhydrous) DMF (Drug Master File) is a document detailing the whole manufacturing process of Doxycycline (anhydrous) active pharmaceutical ingredient (API) in detail. Different forms of Doxycycline (anhydrous) DMFs exist exist since differing nations have different regulations, such as Doxycycline (anhydrous) USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Doxycycline (anhydrous) DMF submitted to regulatory agencies in the US is known as a USDMF. Doxycycline (anhydrous) USDMF includes data on Doxycycline (anhydrous)'s chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Doxycycline (anhydrous) USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Doxycycline (anhydrous) suppliers with USDMF on PharmaCompass.
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