Suanfarma, at the Core of a Better Life.
01 1Suanfarma
02 2Curia
03 3Hovione
04 1IDT Australia Limited
05 2Kyowa Hakko Bio
06 1Nippon Kayaku
07 2Pfizer Inc
08 1UQUIFA
09 1Zhejiang Hisun Pharmaceutical
10 2Zhejiang Medicine Co Ltd
01 1MINOCYCLINE
02 1MINOCYCLINE HYDOCHLORIDE, SAKAI PLANT, OSAKA PREFECTURE JAPAN
03 6MINOCYCLINE HYDROCHLORIDE
04 1MINOCYCLINE HYDROCHLORIDE (DIHYDRATE)
05 1MINOCYCLINE HYDROCHLORIDE (DIHYDRATE) MICRONIZED
06 1MINOCYCLINE HYDROCHLORIDE CAP
07 1MINOCYCLINE HYDROCHLORIDE MICRONIZED
08 4MINOCYCLINE HYDROCHLORIDE USP
01 1Australia
02 3China
03 3Japan
04 3Portugal
05 2Spain
06 4U.S.A
01 10Active
02 6Inactive
01 6Complete
02 10Blank
GDUFA
DMF Review : Complete
Rev. Date : 2013-07-02
Pay. Date : 2013-06-20
DMF Number : 13758
Submission : 1998-09-01
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 33279
Submission : 2018-11-28
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-01-30
Pay. Date : 2013-01-16
DMF Number : 14802
Submission : 2000-03-22
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 34217
Submission : 2019-11-14
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2015-07-29
Pay. Date : 2015-04-28
DMF Number : 29003
Submission : 2015-01-08
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-01-15
Pay. Date : 2012-12-14
DMF Number : 13738
Submission : 1998-09-01
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15014
Submission : 2000-10-02
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 26050
Submission : 2012-07-20
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2019-05-10
Pay. Date : 2018-07-25
DMF Number : 32664
Submission : 2018-05-14
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2022-07-25
Pay. Date : 2022-05-09
DMF Number : 35939
Submission : 2022-04-07
Status : Active
Type : II
A Minocycline manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Minocycline, including repackagers and relabelers. The FDA regulates Minocycline manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Minocycline 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 Minocycline manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Minocycline supplier is an individual or a company that provides Minocycline active pharmaceutical ingredient (API) or Minocycline finished formulations upon request. The Minocycline suppliers may include Minocycline API manufacturers, exporters, distributors and traders.
click here to find a list of Minocycline suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Minocycline DMF (Drug Master File) is a document detailing the whole manufacturing process of Minocycline active pharmaceutical ingredient (API) in detail. Different forms of Minocycline DMFs exist exist since differing nations have different regulations, such as Minocycline USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Minocycline DMF submitted to regulatory agencies in the US is known as a USDMF. Minocycline USDMF includes data on Minocycline's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Minocycline USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Minocycline suppliers with USDMF on PharmaCompass.
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