Vamsi Labs is one of the major manufacturers of Anti-asthmatic, Anti-migraine & Anti-psychotic APIs.
01 1Vamsi Labs
02 1Hosho Co
03 2Opocrin SpA
04 2Otsuka Chemical Co Ltd
05 1Recipharm AB
06 1Shaanxi Dasheng
01 1China
02 1India
03 2Italy
04 3Japan
05 1Sweden
01 2Inactive
02 6Blank
01 8Blank
01 1218MF10948
02 1220MF10003
03 1306MF10056
04 5Blank
01 8Blank
01 120121130-195-I-157-02
02 120121130-195-I-158-01
03 6Blank
01 8Blank
01 8Blank
Vamsi Labs is one of the major manufacturers of Anti-asthmatic, Anti-migraine & Anti-psychotic APIs.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3606
Submission : 1979-09-19
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4820
Submission : 1983-01-17
Status : Inactive
Type : II
Registration Number : 220MF10003
Registrant's Address : 7-30-7 Toshima, Kita-ku, Tokyo
Initial Date of Registration : 2008-01-09
Latest Date of Registration :
Registration Number : 218MF10948
Registrant's Address : Strada Statale dei Giovi, 131-20037 Paderno Dugnano (MI) - Italy
Initial Date of Registration : 2006-11-24
Latest Date of Registration :
Registrant Name : Korea Otsuka Pharmaceutical Co., Ltd.
Registration Date : 2012-11-30
Registration Number : 20121130-195-I-157-02
Manufacturer Name : Otsuka Pharmaceutical Co., Ltd.
Manufacturer Address : 224-18, Hiraishi Ebisuno, Kawauchi-cho, Tokushima-shi, Tokushima, Japan
Registrant Name : Korea Otsuka Pharmaceutical Co., Ltd.
Registration Date : 2012-11-30
Registration Number : 20121130-195-I-158-01
Manufacturer Name : Otsuka Pharmaceutical Co., Ltd.
Manufacturer Address : 224-18, Hiraishi Ebisuno, Kawauchi-cho, Tokushima-shi, Tokushima, Japan
Registration Number : 306MF10056
Registrant's Address : F9 of Jiezuo Square, No. 2 South Fenghui Road, Xi\'an Hi-Tech Industrial Development, Xi\'an, China
Initial Date of Registration : 2024-04-18
Latest Date of Registration :
100
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A CI888 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CI888, including repackagers and relabelers. The FDA regulates CI888 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CI888 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 CI888 supplier is an individual or a company that provides CI888 active pharmaceutical ingredient (API) or CI888 finished formulations upon request. The CI888 suppliers may include CI888 API manufacturers, exporters, distributors and traders.
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