European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.

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01 1Polpharma
02 1Interquim SA
03 1Biophore India Pharmaceuticals Pvt Ltd
04 1Bajaj Healthcare
05 1Dasami Lab
06 1Guangzhou Tosun Pharmaceutical
07 1Hy-Gro Chemicals
08 1Jiangsu Tasly Diyi Pharmaceutical Co., Ltd. CN 223 002 Huai'an
09 1Livzon New North River Pharmaceutical
10 1MSN Laboratories
11 1Natco Pharma
12 1Nifty Labs
13 1SMS Pharmaceuticals
14 1ScinoPharm Taiwan Ltd
15 1Sichuan Taienkang Pharmaceutical
16 1Zydus Lifesciences
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01 4China
02 9India
03 1Poland
04 1Spain
05 1Taiwan
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01 6Active
02 1Inactive
03 9Blank
01 16Blank
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01 16Blank
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01 1WC-0383
02 15Blank
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01 16Blank
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01 169766-056
02 170966-0018
03 173435-002
04 13Blank
01 16Blank
European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.
Interquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 34415
Submission : 2019-12-28
Status : Active
Type : II
NDC Package Code : 73435-002
Start Marketing Date : 2019-12-09
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 37430
Submission : 2022-12-16
Status : Active
Type : II

GDUFA
DMF Review : Reviewed
Rev. Date : 2020-03-20
Pay. Date : 2020-01-27
DMF Number : 34354
Submission : 2020-02-04
Status : Active
Type : II
NDC Package Code : 70966-0018
Start Marketing Date : 2018-06-28
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 34289
Submission : 2019-12-04
Status : Inactive
Type : II





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A NUPLAZID manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of NUPLAZID, including repackagers and relabelers. The FDA regulates NUPLAZID manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. NUPLAZID 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 NUPLAZID supplier is an individual or a company that provides NUPLAZID active pharmaceutical ingredient (API) or NUPLAZID finished formulations upon request. The NUPLAZID suppliers may include NUPLAZID API manufacturers, exporters, distributors and traders.
click here to find a list of NUPLAZID suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
We have 16 companies offering NUPLAZID
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