Bioquim: An European GMP-certified company manufacturing bulk APIs, specializing in sterile lyophilization and chemical synthesis.

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01 1Bioquim
02 1Basic Nutrition
03 1Willow Birch Pharma
04 1Beijing Mesochem Technology
05 1Sumar Biotech
06 1Anlon Healthcare Ltd
07 2Actylis
08 1Anmol Chemicals
09 1Biopeptek Pharmaceuticals
10 1Ceyone Life Sciences
11 1Chongqing DaXin Pharmaceutical
12 1Gurvey & Berry
13 1Hanways Chempharm
14 1Jin Dun Medical
15 1KOHJIN BIO
16 1Kaiping Genuine Biochemical Pharmaceutical
17 2Kyowa Hakko Bio
18 1Mac-Chem Products (India) Pvt.Ltd
19 1Pcca
20 2SIGMA TAU
21 2Shandong Jincheng Pharm.&Chem
22 1Shandong Keyuan Pharmaceutical
23 2Shenzhen GSH Bio-tech Co., Ltd
24 1Spectrum Chemical
25 1Summit Ingredients
26 1Xian Tian Guangyuan Biotech
27 1Zhejiang Hisun Chemical Co., Ltd.
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01 1Canada
02 14China
03 5India
04 3Japan
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06 7U.S.A
07 1United Kingdom
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01 3Active
02 5Inactive
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01 2Valid
02 1Withdrawn by Holder
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01 1217MF10240
02 1217MF10303
03 1223MF10160
04 1304MF10007
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01 120200629-211-J-663
02 120200629-211-J-663(1)
03 120250623-210-J-1927
04 120250623-210-J-1927(1)
05 120250623-210-J-1927(A)
06 120250728-211-J-1963
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01 112497-1054
02 149452-3352
03 151927-5100
04 173083-001
05 173083-002
06 173212-107
07 183589-116
08 185207-017
09 185297-103
10 185368-001
11 185756-101
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Bioquim: An European GMP-certified company manufacturing bulk APIs, specializing in sterile lyophilization and chemical synthesis.
Willow Birch Pharma delivers trusted, high-quality APIs nationwide with unmatched service, compliance, and competitive value.
Anlon Healthcare manufactures high-quality Pharmaceutical Bulk Drugs & Intermediates compliant with FDA, PMDA, KFDA, cGMP & WHO-GMP.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 41240
Submission : 2025-01-24
Status : Active
Type : IV

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3043
Submission : 1977-10-21
Status : Inactive
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4278
Submission : 1981-09-17
Status : Inactive
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2562
Submission : 1975-11-13
Status : Inactive
Type : II

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A Tathion manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tathion, including repackagers and relabelers. The FDA regulates Tathion manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tathion API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Tathion supplier is an individual or a company that provides Tathion active pharmaceutical ingredient (API) or Tathion finished formulations upon request. The Tathion suppliers may include Tathion API manufacturers, exporters, distributors and traders.
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