TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.

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01 2TAPI Technology & API Services
02 1Abbott Laboratories
03 1Alembic Pharmaceuticals Limited
04 1Amano Enzyme
05 1Artemis Biotech
06 2Biocon
07 3Chongqing DaXin Pharmaceutical
08 1Concord Biotech
09 1Darmerica
10 2Ercros
11 1Freemen Nutra
12 1HENAN TOPFOND PHARMACEUTICAL Co,. Ltd
13 1Krebs Biochemicals & Industries Ltd
14 1Krka
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16 1Livzon Group Fuzhou Fuxing Pharmaceutical Co., Ltd.
17 1Livzon New North River Pharmaceutical
18 3Lupin Ltd
19 1Merck & Co
20 1Qingdao Qingmei Biotech
21 2Recordati
22 1Sterling Biotech
23 2Sun Pharmaceutical Industries Limited
24 1Symbio
25 1Syngen Biotech
26 2Teva Pharmaceutical Industries
27 1Tocopharm Co. Limited
28 1Yung Shin Pharm Industrial
29 1Zhejiang Apeloa Kangyu Pharmaceutical Co. Ltd
30 1Zhejiang Hisun Chemical Co., Ltd.
31 1Zhejiang Hisun Pharmaceutical
32 2Zhejiang Ruibang Laboratories
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01 15China
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06 2Spain
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08 3U.S.A
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01 10Active
02 20Inactive
03 14Blank
01 5Valid
02 7Withdrawn by Holder
03 32Blank
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01 1217MF10683
02 43Blank
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01 1WC-0201
02 1WC-0292
03 1WC-0379
04 41Blank
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01 120051213-7-B-210-05
02 120051213-7-B-210-05(1)
03 42Blank
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01 120076-0402
02 151846-1014
03 151846-1040
04 257885-0008
05 158623-0021
06 171052-668
07 184671-1014
08 184671-1040
09 35Blank
01 44Blank
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
GDUFA
DMF Review : Reviewed
Rev. Date : 2012-12-27
Pay. Date : 2012-12-03
DMF Number : 11502
Submission : 1995-05-12
Status : Active
Type : II
Certificate Number : CEP 2000-406 - Rev 06
Issue Date : 2025-07-08
Type : Chemical
Substance Number : 1538
Status : Valid
NDC Package Code : 84671-1014
Start Marketing Date : 2019-08-16
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
| Available Reg Filing : ASMF |
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
NDC Package Code : 84671-1040
Start Marketing Date : 2013-01-11
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
| Available Reg Filing : ASMF |
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 24859
Submission : 2011-04-07
Status : Active
Type : II
Certificate Number : R1-CEP 2014-146 - Rev 00
Issue Date : 2020-03-16
Type : Chemical
Substance Number : 1538
Status : Valid
Date of Issue : 2024-02-28
Valid Till : 2026-12-16
Written Confirmation Number : WC-0292
Address of the Firm :

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19217
Submission : 2006-03-01
Status : Active
Type : II

GDUFA
DMF Review : Reviewed
Rev. Date : 2012-12-26
Pay. Date : 2012-11-15
DMF Number : 12133
Submission : 1996-09-17
Status : Active
Type : II
Certificate Number : R1-CEP 2001-406 - Rev 05
Issue Date : 2021-07-02
Type : Chemical
Substance Number : 1538
Status : Valid
NDC Package Code : 58623-0021
Start Marketing Date : 1996-09-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14402
Submission : 1999-09-15
Status : Inactive
Type : II
Certificate Number : R0-CEP 2005-140 - Rev 00
Issue Date : 2007-12-07
Type : Chemical
Substance Number : 1538
Status : Withdrawn by Holder

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17662
Submission : 2004-09-08
Status : Inactive
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 12481
Submission : 1997-04-25
Status : Inactive
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 12400
Submission : 1997-03-02
Status : Inactive
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 18188
Submission : 2005-03-15
Status : Inactive
Type : II

17
PharmaCompass offers a list of Lovastatin API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Lovastatin manufacturer or Lovastatin supplier for your needs.
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A Tox21_300268 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_300268, including repackagers and relabelers. The FDA regulates Tox21_300268 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_300268 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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