01 1Recipharm AB
02 1Blank
01 2TULOBUTEROL BASE
01 1Sweden
02 1Blank
01 1Active
02 1Inactive
01 2Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 21750
Submission : 2008-06-27
Status : Active
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6648
Submission : 1986-10-17
Status : Inactive
Type : II
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PharmaCompass offers a list of Tulobuterol API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Tulobuterol manufacturer or Tulobuterol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tulobuterol manufacturer or Tulobuterol supplier.
A Hokunalin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hokunalin, including repackagers and relabelers. The FDA regulates Hokunalin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hokunalin 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 Hokunalin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Hokunalin supplier is an individual or a company that provides Hokunalin active pharmaceutical ingredient (API) or Hokunalin finished formulations upon request. The Hokunalin suppliers may include Hokunalin API manufacturers, exporters, distributors and traders.
click here to find a list of Hokunalin suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Hokunalin DMF (Drug Master File) is a document detailing the whole manufacturing process of Hokunalin active pharmaceutical ingredient (API) in detail. Different forms of Hokunalin DMFs exist exist since differing nations have different regulations, such as Hokunalin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Hokunalin DMF submitted to regulatory agencies in the US is known as a USDMF. Hokunalin USDMF includes data on Hokunalin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Hokunalin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Hokunalin suppliers with USDMF on PharmaCompass.
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