Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.
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01 1Centrient Pharmaceuticals
02 1ADL BioPharma
03 1Bristol Laboratories Ltd
04 1CSPC Pharmaceutical Group
05 1Chemopharma GmbH
06 1Fengchen Group
07 1JIANGXI DONGFENG PHARMACEUTICAL LLC
08 1Novartis Pharmaceuticals Corporation
09 1Pfizer Inc
10 1RR LIFESCIENCES
11 1Reyoung pharmaceutical
12 2Sandoz B2B
13 1Vega
14 1Wyeth Pharmaceuticals Inc
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01 1Austria
02 5China
03 1India
04 1Netherlands
05 1Spain
06 3Switzerland
07 2U.S.A
08 1United Kingdom
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01 1Active
02 3Inactive
03 11Blank
01 1Valid
02 1Withdrawn by Holder
03 13Blank
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01 1219MF10336
02 1220MF10136
03 13Blank
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01 15Blank
Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.
GDUFA
DMF Review : Reviewed
Rev. Date : 2018-04-19
Pay. Date : 2018-03-23
DMF Number : 13294
Submission : 1998-09-01
Status : Active
Type : II
Certificate Number : R1-CEP 2001-066 - Rev 05
Issue Date : 2023-07-26
Type : Chemical
Substance Number : 373
Status : Valid
NDC Package Code : 43858-510
Start Marketing Date : 2010-02-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (10kg/10kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13328
Submission : 1998-09-01
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13655
Submission : 1998-09-01
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13318
Submission : 1998-09-01
Status : Inactive
Type : II
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
Registration Number : 220MF10136
Registrant's Address : Industrypark Hoechst Brueningstrasse 50 D-65929 Frankfurt am Main Germany
Initial Date of Registration : 2008-05-29
Latest Date of Registration :
Registration Number : 219MF10336
Registrant's Address : 15 Dongfeng Rd. , Leping City, Jiangxi Province, China
Initial Date of Registration : 2007-11-21
Latest Date of Registration :
NDC Package Code : 70847-723
Start Marketing Date : 2016-08-09
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
Certificate Number : R1-CEP 1994-018 - Rev 04
Issue Date : 2004-12-01
Type : Chemical
Substance Number : 373
Status : Withdrawn by Holder
NDC Package Code : 43858-510
Start Marketing Date : 2010-02-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (10kg/10kg)
Marketing Category : BULK INGREDIENT
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A Penicillin G Benzathine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Penicillin G Benzathine, including repackagers and relabelers. The FDA regulates Penicillin G Benzathine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Penicillin G Benzathine 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 Penicillin G Benzathine supplier is an individual or a company that provides Penicillin G Benzathine active pharmaceutical ingredient (API) or Penicillin G Benzathine finished formulations upon request. The Penicillin G Benzathine suppliers may include Penicillin G Benzathine API manufacturers, exporters, distributors and traders.
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We have 14 companies offering Penicillin G Benzathine
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