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01 1Nanhai Beisha Pharmaceutical
02 1SHANGHAI ZHONGXI SUNVE PHARMACEUTICAL
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01 2China
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01 1Inactive
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01 163422-704
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01 15153
02 15756
03 16181
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USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4575
Submission : 1982-04-29
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
VMF Number : 5153
Submission : 1987-02-09
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
NDC Package Code : 63422-704
Start Marketing Date : 2016-06-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
VMF Number : 6181
Submission : 2017-02-22
Status : Active
Type : II
VMF Number : 5756
Submission : 2002-12-09
Status : Inactive
Type : II
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A Tox21_300894 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_300894, including repackagers and relabelers. The FDA regulates Tox21_300894 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_300894 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Tox21_300894 supplier is an individual or a company that provides Tox21_300894 active pharmaceutical ingredient (API) or Tox21_300894 finished formulations upon request. The Tox21_300894 suppliers may include Tox21_300894 API manufacturers, exporters, distributors and traders.
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