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01 1Curia
02 1Guangzhou Tosun Pharmaceutical
03 1Johnson & Johnson Innovative Medicine
04 3Katsura Chemical
05 1Yonsung Fine Chemicals
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01 1China
02 3Japan
03 1South Korea
04 2U.S.A
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01 1Inactive
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01 4Valid
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01 1218MF10995
02 1228MF10206
03 1230MF10168
04 1306MF10125
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01 165089-0042
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GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5847
Submission : 1985-04-19
Status : Inactive
Type : II
Certificate Number : R1-CEP 2002-147 - Rev 03
Issue Date : 2020-12-09
Type : Chemical
Substance Number : 1484
Status : Valid
Registration Number : 228MF10206
Registrant's Address : Turnhoutseweg 30 B-2340 Beerse Belgium
Initial Date of Registration : 2016-11-02
Latest Date of Registration :
Certificate Number : CEP 2018-217 - Rev 01
Issue Date : 2024-09-02
Type : Chemical
Substance Number : 1484
Status : Valid
Registration Number : 306MF10125
Registrant's Address : 4-15-19 Hibarigaoka, Zama City, Kanagawa Prefecture
Initial Date of Registration : 2024-09-11
Latest Date of Registration :
Certificate Number : R1-CEP 2014-277 - Rev 00
Issue Date : 2021-10-27
Type : Chemical
Substance Number : 1484
Status : Valid
Registration Number : 230MF10168
Registrant's Address : 4-15-19 Hibarigaoka, Zama City, Kanagawa Prefecture
Initial Date of Registration : 2018-12-19
Latest Date of Registration :
Registration Number : 218MF10995
Registrant's Address : 4-15-19 Hibarigaoka, Zama City, Kanagawa Prefecture
Initial Date of Registration : 2006-12-18
Latest Date of Registration :
Certificate Number : R1-CEP 2012-002 - Rev 04
Issue Date : 2021-11-16
Type : Chemical
Substance Number : 1484
Status : Valid
NDC Package Code : 65089-0042
Start Marketing Date : 1993-11-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Levocabastine 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 Levocabastine manufacturer or Levocabastine supplier for your needs.
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A livocab manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of livocab, including repackagers and relabelers. The FDA regulates livocab manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. livocab 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 livocab supplier is an individual or a company that provides livocab active pharmaceutical ingredient (API) or livocab finished formulations upon request. The livocab suppliers may include livocab API manufacturers, exporters, distributors and traders.
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We have 5 companies offering livocab
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