Midas Pharma provides expertise in developing and supplying APIs, finished products, and intermediates.
01 1Midas Pharma
02 1Bachem AG
03 1Biosynth AG
04 1Guangzhou Tosun Pharmaceutical
05 1Heraeus Holding
06 1Jiangsu Lianhuan Pharmaceutical
07 1Juzen Chemical Corporation
08 1MEDAC GESELLSCHAFT FUR KLINISCHE SPEZIALPRAPARATE MBH
09 1Nihon Rikagaku
10 1Nippon Rikagaku Yakuhin
01 2China
02 3Germany
03 3Japan
04 2Switzerland
01 3Active
02 3Inactive
03 4Blank
01 10Blank
01 1224MF10095
02 1229MF10010
03 8Blank
01 10Blank
Midas Pharma provides expertise in developing and supplying APIs, finished products, and intermediates.
GDUFA
DMF Review : N/A
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DMF Number : 29376
Submission : 2015-05-27
Status : Active
Type : II
Available Reg Filing : ASMF, CH, TR |
Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
GDUFA
DMF Review : N/A
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DMF Number : 9972
Submission : 1992-11-25
Status : Active
Type : II
NDC Package Code : 51504-0005
Start Marketing Date : 1992-11-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Daewoong Pharmaceutical Co., Ltd.
Registration Date : 2007-09-28
Registration Number : 43-2-ND
Manufacturer Name : Sochinaz SA
Manufacturer Address : Route du Simplon 22 CH-1895 Vionnaz, Switzerland
GDUFA
DMF Review : N/A
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DMF Number : 24359
Submission : 2010-11-12
Status : Active
Type : II
Registration Number : 224MF10095
Registrant's Address : Heraeusstr. 12-14; 63450 Hanau; Germany
Initial Date of Registration : 2012-04-27
Latest Date of Registration : --
GDUFA
DMF Review : N/A
Rev. Date :
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DMF Number : 24562
Submission : 2010-12-27
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
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DMF Number : 17844
Submission : 2004-11-15
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 23711
Submission : 2010-04-06
Status : Inactive
Type : II
Registration Number : 229MF10010
Registrant's Address : 2-2 Nihonbashi Honcho 4-chome, Chuo-ku, Tokyo
Initial Date of Registration : 2017-01-18
Latest Date of Registration : --
A Aminolevulinic Acid Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aminolevulinic Acid Hydrochloride, including repackagers and relabelers. The FDA regulates Aminolevulinic Acid Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aminolevulinic Acid Hydrochloride 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 Aminolevulinic Acid Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Aminolevulinic Acid Hydrochloride supplier is an individual or a company that provides Aminolevulinic Acid Hydrochloride active pharmaceutical ingredient (API) or Aminolevulinic Acid Hydrochloride finished formulations upon request. The Aminolevulinic Acid Hydrochloride suppliers may include Aminolevulinic Acid Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Aminolevulinic Acid Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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