Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
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01 1Biophore India Pharmaceuticals Pvt Ltd
02 1LGM Pharma
03 1Bioiberica
04 1AASraw Biochemical Technology Co., Ltd
05 1Anhui Biochem United Pharmaceutical
06 2Apotex Pharmachem
07 2Aurore Life Sciences
08 1Azico Biophore India Pvt. Ltd
09 1Biotechnica DWC
10 1Bracco
11 1Fareva
12 1GLAND PHARMA LIMITED
13 1Guangzhou Tosun Pharmaceutical
14 1Innova Remedies
15 1Laurus Labs
16 1Lupin Ltd
17 1MSN Laboratories
18 2Macleods Pharmaceuticals Limited
19 1Peptido GmbH
20 1Rakshit Drugs
21 1Rhodia Organique SAS
22 1SAFC
23 1Sandoz B2B
24 2Blank
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01 1Algeria
02 2Canada
03 3China
04 1France
05 1Germany
06 12India
07 1Italy
08 1Luxembourg
09 1Spain
10 1Switzerland
11 2U.S.A
12 2Blank
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01 11Active
02 4Inactive
03 13Blank
01 10Valid
02 18Blank
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01 1217MF10456
02 1221MF10168
03 26Blank
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01 1WC-0119
02 1WC-0119A6
03 1WC-0330
04 1WC-0404A3
05 1WC-0427A3-4
06 23Blank
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
Bioiberica is a global life science company committed to improving the health & wellbeing of people, animals & plants.
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 38129
Submission : 2023-05-06
Status : Active
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 29526
Submission : 2015-06-29
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2015-09-25
Pay. Date : 2015-08-17
DMF Number : 29550
Submission : 2015-07-27
Status : Active
Type : II
Date of Issue : 2022-08-04
Valid Till : 2025-03-04
Written Confirmation Number : WC-0427A3-4
Address of the Firm :
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 38710
Submission : 2023-09-29
Status : Active
Type : II
NDC Package Code : 54893-0125
Start Marketing Date : 2023-09-29
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-01-30
Pay. Date : 2013-01-15
DMF Number : 14715
Submission : 2000-02-01
Status : Active
Type : II
Certificate Number : R1-CEP 1998-048 - Rev 06
Issue Date : 2023-07-05
Type : Chemical
Substance Number : 401
Status : Valid
Registration Number : 221MF10168
Registrant's Address : Am Kraftwerk 6, D-66450 Bexbach, Germany
Initial Date of Registration : 2009-07-30
Latest Date of Registration :
NDC Package Code : 67891-001
Start Marketing Date : 2003-04-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Registrant Name : Samnam Pharmaceutical Co., Ltd.
Registration Date : 2020-01-10
Registration Number : 20181023-209-J-104(3)
Manufacturer Name : Peptido GmbH
Manufacturer Address : Am Kraftwerk 6, 66450 Bexbach, Germany
GDUFA
DMF Review : Reviewed
Rev. Date : 2014-06-23
Pay. Date : 2013-09-26
DMF Number : 24402
Submission : 2011-10-20
Status : Active
Type : II
Certificate Number : CEP 2011-315 - Rev 02
Issue Date : 2023-11-08
Type : Chemical
Substance Number : 401
Status : Valid
NDC Package Code : 46014-1013
Start Marketing Date : 2011-10-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-01-15
Pay. Date : 2012-12-21
DMF Number : 4789
Submission : 1983-01-06
Status : Active
Type : II
Certificate Number : CEP 1998-141 - Rev 11
Issue Date : 2023-09-26
Type : Chemical
Substance Number : 401
Status : Valid
Registration Number : 217MF10456
Registrant's Address : Biochemiesstrasse 10, 6250 Kundl, Austria
Initial Date of Registration : 2005-08-24
Latest Date of Registration :
NDC Package Code : 43858-410
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 : Reviewed
Rev. Date : 2021-10-12
Pay. Date : 2021-08-06
DMF Number : 34044
Submission : 2019-08-05
Status : Active
Type : II
Certificate Number : CEP 2023-295 - Rev 00
Issue Date : 2023-12-11
Type : Chemical
Substance Number : 401
Status : Valid
Date of Issue : 2022-09-19
Valid Till : 2025-07-02
Written Confirmation Number : WC-0119
Address of the Firm :
NDC Package Code : 72761-026
Start Marketing Date : 2023-12-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2015-07-10
Pay. Date : 2015-05-05
DMF Number : 29098
Submission : 2015-03-14
Status : Active
Type : II
Certificate Number : R1-CEP 2016-280 - Rev 01
Issue Date : 2023-05-26
Type : Chemical
Substance Number : 401
Status : Valid
Date of Issue : 2021-02-26
Valid Till : 2023-06-22
Written Confirmation Number : WC-0404A3
Address of the Firm :
NDC Package Code : 69575-4001
Start Marketing Date : 2015-11-24
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (20kg/20kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Aging Life Science Co., Ltd.
Registration Date : 2020-11-25
Registration Number : 20201125-209-J-789
Manufacturer Name : Azico Biophore India Private Limited
Manufacturer Address : Plot Number 40/A, Sy. No. 13,15,16,51,52 & 182, JN.Pharma city, Thanam(V), Anakapalli District 531021, Andhra Pradesh, India
GDUFA
DMF Review : Reviewed
Rev. Date : 2016-04-13
Pay. Date : 2016-03-18
DMF Number : 30376
Submission : 2016-03-22
Status : Active
Type : II
Certificate Number : CEP 2017-048 - Rev 01
Issue Date : 2023-12-05
Type : Chemical
Substance Number : 401
Status : Valid
Date of Issue : 2019-07-26
Valid Till : 2022-04-07
Written Confirmation Number : WC-0330
Address of the Firm :
NDC Package Code : 57297-977
Start Marketing Date : 2019-12-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2017-03-23
Pay. Date : 2017-03-06
DMF Number : 31203
Submission : 2017-01-31
Status : Active
Type : II
Certificate Number : CEP 2023-227 - Rev 00
Issue Date : 2024-02-01
Type : Chemical
Substance Number : 401
Status : Valid
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7374
Submission : 1988-03-07
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14256
Submission : 1999-06-29
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 25818
Submission : 2012-02-20
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 30113
Submission : 2016-03-01
Status : Inactive
Type : II
Certificate Number : R1-CEP 2010-011 - Rev 01
Issue Date : 2017-03-06
Type : Chemical
Substance Number : 401
Status : Valid
Certificate Number : R1-CEP 2017-040 - Rev 00
Issue Date : 2023-04-03
Type : Chemical
Substance Number : 401
Status : Valid
Certificate Number : R0-CEP 2019-190 - Rev 01
Issue Date : 2023-05-31
Type : Chemical
Substance Number : 401
Status : Valid
Date of Issue : 2020-08-07
Valid Till : 2022-07-02
Written Confirmation Number : WC-0119A6
Address of the Firm :
NDC Package Code : 72761-026
Start Marketing Date : 2023-12-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
24
PharmaCompass offers a list of Levothyroxine Sodium 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 Levothyroxine Sodium manufacturer or Levothyroxine Sodium supplier for your needs.
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A Levothyroxine Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Levothyroxine Sodium, including repackagers and relabelers. The FDA regulates Levothyroxine Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Levothyroxine Sodium 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 Levothyroxine Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Levothyroxine Sodium supplier is an individual or a company that provides Levothyroxine Sodium active pharmaceutical ingredient (API) or Levothyroxine Sodium finished formulations upon request. The Levothyroxine Sodium suppliers may include Levothyroxine Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Levothyroxine Sodium suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
We have 23 companies offering Levothyroxine Sodium
Get in contact with the supplier of your choice: