HRV Global Life Sciences - Market Expansion Leader in Pharmaceuticals.
01 1HRV Global Life Sciences
02 1Tagoor Laboratories
03 1Actavis Inc
04 1Aspire Lifesciences Pvt Ltd
05 1Centaur Pharmaceuticals
06 1Dipharma
07 1Nishchem International Pvt. Ltd
08 1Olon S.p.A
09 2R L Fine Chem
10 1SAFC
11 1Sifavitor srl
12 1Vasudha Pharma Chem
13 2elm-plastic GmbH
14 1Blank
01 2Germany
02 8India
03 1Ireland
04 3Italy
05 1U.S.A
06 1Blank
01 5Active
02 5Inactive
03 6Blank
01 4Valid
02 12Blank
01 1219MF10264
02 15Blank
01 1WC-0107
02 1WC-0139
03 1WC-0445A1
04 13Blank
Tagoor's product development expertise, backed by our comprehensive understanding of the processes, helps us offer high-quality APIs.
GDUFA
DMF Review : Reviewed
Rev. Date : 2019-05-20
Pay. Date : 2019-01-28
DMF Number : 31974
Submission : 2017-09-08
Status : Active
Type : II
Certificate Number : R1-CEP 2017-066 - Rev 00
Issue Date : 2023-07-31
Type : Chemical
Substance Number : 941
Status : Valid
NDC Package Code : 66577-025
Start Marketing Date : 1984-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
GDUFA
DMF Review : Reviewed
Rev. Date : 2023-10-23
Pay. Date : 2023-08-08
DMF Number : 33227
Submission : 2018-09-29
Status : Active
Type : II
Certificate Number : CEP 2014-032 - Rev 02
Issue Date : 2024-06-28
Type : Chemical
Substance Number : 941
Status : Valid
Date of Issue : 2020-02-14
Valid Till : 2022-07-28
Written Confirmation Number : WC-0445A1
Address of the Firm :
NDC Package Code : 71554-011
Start Marketing Date : 2019-04-27
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 : 21330
Submission : 2008-01-31
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7414
Submission : 1988-03-30
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2018-12-28
Pay. Date : 2015-04-09
DMF Number : 7846
Submission : 1988-12-29
Status : Active
Type : II
Registration Number : 219MF10264
Registrant's Address : Via Bissone, 5, 20021-Baranzate, Milano, Italy
Initial Date of Registration : 2007-08-16
Latest Date of Registration : --
NDC Package Code : 46438-0049
Start Marketing Date : 2012-03-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Toru Corporation
Registration Date : 2024-11-12
Registration Number : 20241112-209-J-1722
Manufacturer Name : Dipharma Francis Srl
Manufacturer Address : Via Bissone, 5, 20021, Baranzate (MI), Italy
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 25380
Submission : 2011-10-07
Status : Inactive
Type : II
Certificate Number : CEP 2006-026 - Rev 02
Issue Date : 2023-10-19
Type : Chemical
Substance Number : 941
Status : Valid
Date of Issue : 2022-06-08
Valid Till : 2025-06-25
Written Confirmation Number : WC-0107
Address of the Firm :
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3291
Submission : 1978-09-15
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2890
Submission : 1977-03-18
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2891
Submission : 1977-03-18
Status : Inactive
Type : II
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 : 8143
Submission : 1989-07-26
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Date of Issue : 2019-07-22
Valid Till : 2022-07-22
Written Confirmation Number : WC-0139
Address of the Firm :
NDC Package Code : 71554-011
Start Marketing Date : 2019-04-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Certificate Number : R1-CEP 2013-070 - Rev 02
Issue Date : 2023-05-31
Type : Chemical
Substance Number : 941
Status : Valid
NDC Package Code : 17337-0534
Start Marketing Date : 2020-03-03
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER ()
Marketing Category : BULK INGREDIENT
A Nortriptyline Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nortriptyline Hydrochloride, including repackagers and relabelers. The FDA regulates Nortriptyline Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nortriptyline Hydrochloride 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 Nortriptyline Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nortriptyline Hydrochloride supplier is an individual or a company that provides Nortriptyline Hydrochloride active pharmaceutical ingredient (API) or Nortriptyline Hydrochloride finished formulations upon request. The Nortriptyline Hydrochloride suppliers may include Nortriptyline Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Nortriptyline Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
We have 13 companies offering Nortriptyline Hydrochloride
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