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 1Biopeptek Pharmaceuticals
08 3Chongqing DaXin Pharmaceutical
09 1Concord Biotech
10 1Darmerica
11 2Ercros
12 1Freemen Nutra
13 1HENAN TOPFOND PHARMACEUTICAL Co,. Ltd
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17 1Livzon Group Fuzhou Fuxing Pharmaceutical Co., Ltd.
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19 3Lupin Ltd
20 1Merck & Co
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24 2Sun Pharmaceutical Industries Limited
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01 15China
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08 4U.S.A
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01 9Active
02 21Inactive
03 15Blank
01 5Valid
02 7Withdrawn by Holder
03 33Blank
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01 1217MF10683
02 44Blank
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01 1WC-0201
02 1WC-0292
03 1WC-0379
04 42Blank
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01 120051213-7-B-210-05
02 120051213-7-B-210-05(1)
03 43Blank
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01 120076-0402
02 151846-1014
03 151846-1040
04 257885-0008
05 158623-0021
06 171052-668
07 173212-215
08 184671-1014
09 184671-1040
10 35Blank
01 45Blank
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.
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 : 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 : 12133
Submission : 1996-09-17
Status : Inactive
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 : 2027-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT

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

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PharmaCompass offers a list of Lovastatin API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Lovastatin manufacturer or Lovastatin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Lovastatin manufacturer or Lovastatin supplier.
A Mevacor manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mevacor, including repackagers and relabelers. The FDA regulates Mevacor manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mevacor API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Mevacor manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Mevacor supplier is an individual or a company that provides Mevacor active pharmaceutical ingredient (API) or Mevacor finished formulations upon request. The Mevacor suppliers may include Mevacor API manufacturers, exporters, distributors and traders.
click here to find a list of Mevacor suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
We have 33 companies offering Mevacor
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