01 2Priti Industries
02 2Tomita Pharmaceutical
03 1Blank
01 1ALUMINIUM HYDROXIDE MAGNESIUM CARBONATE CO-DRIED GEL
02 1ALUMINUM HYDROXIDE GEL
03 1DRIED ALUMINIUM HYDROXIDE GEL IP/BP/USP
04 2DRIED ALUMINUM HYDROXIDE GEL
01 2India
02 2Japan
03 1Blank
01 3Active
02 2Inactive
01 5Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 38885
Submission : 2023-11-18
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 38895
Submission : 2023-11-18
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 21384
Submission : 2008-02-21
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8222
Submission : 1989-09-20
Status : Inactive
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 39719
Submission : 2024-04-22
Status : Active
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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PharmaCompass offers a list of Aluminium Hydroxide 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 Aluminium Hydroxide manufacturer or Aluminium Hydroxide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Aluminium Hydroxide manufacturer or Aluminium Hydroxide supplier.
A ALUMINUM HYDROXIDE GEL, DRIED [II] manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ALUMINUM HYDROXIDE GEL, DRIED [II], including repackagers and relabelers. The FDA regulates ALUMINUM HYDROXIDE GEL, DRIED [II] manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ALUMINUM HYDROXIDE GEL, DRIED [II] 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 ALUMINUM HYDROXIDE GEL, DRIED [II] manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A ALUMINUM HYDROXIDE GEL, DRIED [II] supplier is an individual or a company that provides ALUMINUM HYDROXIDE GEL, DRIED [II] active pharmaceutical ingredient (API) or ALUMINUM HYDROXIDE GEL, DRIED [II] finished formulations upon request. The ALUMINUM HYDROXIDE GEL, DRIED [II] suppliers may include ALUMINUM HYDROXIDE GEL, DRIED [II] API manufacturers, exporters, distributors and traders.
click here to find a list of ALUMINUM HYDROXIDE GEL, DRIED [II] suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A ALUMINUM HYDROXIDE GEL, DRIED [II] DMF (Drug Master File) is a document detailing the whole manufacturing process of ALUMINUM HYDROXIDE GEL, DRIED [II] active pharmaceutical ingredient (API) in detail. Different forms of ALUMINUM HYDROXIDE GEL, DRIED [II] DMFs exist exist since differing nations have different regulations, such as ALUMINUM HYDROXIDE GEL, DRIED [II] USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A ALUMINUM HYDROXIDE GEL, DRIED [II] DMF submitted to regulatory agencies in the US is known as a USDMF. ALUMINUM HYDROXIDE GEL, DRIED [II] USDMF includes data on ALUMINUM HYDROXIDE GEL, DRIED [II]'s chemical properties, information on the facilities and procedures used, and details about packaging and storage. The ALUMINUM HYDROXIDE GEL, DRIED [II] USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of ALUMINUM HYDROXIDE GEL, DRIED [II] suppliers with USDMF on PharmaCompass.
We have 2 companies offering ALUMINUM HYDROXIDE GEL, DRIED [II]
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