LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
01 1LGM Pharma
02 1Jai Radhe Sales
03 1Virupaksha Organics
04 1HRV Global Life Sciences
05 1FDC
06 1Fleming Laboratories
07 1Hikal
08 1Johnson & Johnson Innovative Medicine
09 1Nishchem International Pvt. Ltd
10 1RR LIFESCIENCES
11 1Rakshit Drugs
12 1Shaanxi Hanjiang pharmaceutical Group Co
13 1Vasudha Pharma Chem
01 1China
02 10India
03 2U.S.A
01 1Active
02 12Blank
01 1Expired
02 5Valid
03 7Blank
01 13Blank
01 1WC-0055
02 1WC-0094nA2A
03 1WC-0191
04 1WC-0229
05 9Blank
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
Date of Issue : 2022-09-16
Valid Till : 2025-07-02
Written Confirmation Number : WC-0191
Address of the Firm :
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 31934
Submission : 2017-09-07
Status : Active
Type : II
Certificate Number : CEP 2003-150 - Rev 03
Issue Date : 2023-09-08
Type : Chemical
Substance Number : 816
Status : Valid
Date of Issue : 2022-06-08
Valid Till : 2025-07-07
Written Confirmation Number : WC-0055
Address of the Firm :
NDC Package Code : 55545-0702
Start Marketing Date : 2017-12-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Certificate Number : R1-CEP 2015-019 - Rev 00
Issue Date : 2022-05-09
Type : Chemical
Substance Number : 816
Status : Valid
Date of Issue : 2022-08-16
Valid Till : 2025-08-13
Written Confirmation Number : WC-0229
Address of the Firm :
Certificate Number : R2-CEP 1994-016 - Rev 03
Issue Date : 2011-10-27
Type : Chemical
Substance Number : 816
Status : Valid
Certificate Number : R1-CEP 2004-271 - Rev 04
Issue Date : 2022-09-07
Type : Chemical
Substance Number : 816
Status : Valid
Date of Issue : 2022-06-14
Valid Till : 2025-09-02
Written Confirmation Number : WC-0094nA2A
Address of the Firm :
Certificate Number : R0-CEP 2001-130 - Rev 01
Issue Date : 2004-12-03
Type : Chemical
Substance Number : 816
Status : Expired
A Cinnarizine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cinnarizine, including repackagers and relabelers. The FDA regulates Cinnarizine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cinnarizine 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 Cinnarizine supplier is an individual or a company that provides Cinnarizine active pharmaceutical ingredient (API) or Cinnarizine finished formulations upon request. The Cinnarizine suppliers may include Cinnarizine API manufacturers, exporters, distributors and traders.
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