Inke S.A: APIs manufacturing plant.
01 1Inke S.A
02 1Almirall
03 1Hovione
04 1MSN Laboratories
01 1ACLIDINIUM BROMIDE
02 1ACLIDINIUM BROMIDE MICRONIZED
03 1ACLIDINIUM BROMIDE [ROUTE CODE "AU"]
04 1LAS 34273
01 1India
02 1Portugal
03 2Spain
01 3Active
02 1Inactive
01 1Complete
02 3Blank
Inke S.A: APIs manufacturing plant.
GDUFA
DMF Review : Complete
Rev. Date : 2023-06-14
Pay. Date : 2023-04-21
DMF Number : 36437
Submission : 2023-03-16
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16926
Submission : 2003-10-17
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 34231
Submission : 2019-12-20
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 28093
Submission : 2014-03-26
Status : Active
Type : II
61
PharmaCompass offers a list of Aclidinium Bromide API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Aclidinium Bromide manufacturer or Aclidinium Bromide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Aclidinium Bromide manufacturer or Aclidinium Bromide supplier.
PharmaCompass also assists you with knowing the Aclidinium Bromide API Price utilized in the formulation of products. Aclidinium Bromide API Price is not always fixed or binding as the Aclidinium Bromide Price is obtained through a variety of data sources. The Aclidinium Bromide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Eklira genuair (TN) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Eklira genuair (TN), including repackagers and relabelers. The FDA regulates Eklira genuair (TN) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Eklira genuair (TN) 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 Eklira genuair (TN) manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Eklira genuair (TN) supplier is an individual or a company that provides Eklira genuair (TN) active pharmaceutical ingredient (API) or Eklira genuair (TN) finished formulations upon request. The Eklira genuair (TN) suppliers may include Eklira genuair (TN) API manufacturers, exporters, distributors and traders.
click here to find a list of Eklira genuair (TN) suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Eklira genuair (TN) DMF (Drug Master File) is a document detailing the whole manufacturing process of Eklira genuair (TN) active pharmaceutical ingredient (API) in detail. Different forms of Eklira genuair (TN) DMFs exist exist since differing nations have different regulations, such as Eklira genuair (TN) USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Eklira genuair (TN) DMF submitted to regulatory agencies in the US is known as a USDMF. Eklira genuair (TN) USDMF includes data on Eklira genuair (TN)'s chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Eklira genuair (TN) USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Eklira genuair (TN) suppliers with USDMF on PharmaCompass.
We have 4 companies offering Eklira genuair (TN)
Get in contact with the supplier of your choice:
