Vamsi Labs is one of the major manufacturers of Anti-asthmatic, Anti-migraine & Anti-psychotic APIs.
01 1Vamsi Labs
02 1LGM Pharma
03 1DKSH
04 1Jai Radhe Sales
05 1Nortec Quimica
06 1TAPI Technology & API Services
07 1Abbott Laboratories
08 1Fareva
09 1GD Searle LLC
10 1Heumann
11 2Johnson & Johnson Innovative Medicine
12 1MSN Laboratories
13 1Maiden Group
14 1Mankind Pharma
15 1Olon S.p.A
16 1RPG Life Sciences
17 1Sicor Societa Italiana Corticosteroidi Srl
18 1Sifavitor srl
19 1Teva Pharmaceutical Industries
20 1Wuhan Biet
21 2Blank
01 1Brazil
02 1China
03 1Germany
04 6India
05 2Israel
06 3Italy
07 1Luxembourg
08 1Switzerland
09 5U.S.A
10 2Blank
01 7Active
02 6Inactive
03 10Blank
01 5Valid
02 1Withdrawn by Holder
03 17Blank
01 1219MF10333
02 1221MF10041
03 21Blank
01 1WC-0056
02 1WC-0155
03 1WC-0383A6
04 20Blank
Vamsi Labs is one of the major manufacturers of Anti-asthmatic, Anti-migraine & Anti-psychotic APIs.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 34283
Submission : 2019-11-14
Status : Active
Type : II
Certificate Number : R0-CEP 2020-149 - Rev 00
Issue Date : 2023-04-04
Type : Chemical
Substance Number : 616
Status : Valid
Date of Issue : 2022-06-13
Valid Till : 2025-07-02
Written Confirmation Number : WC-0155
Address of the Firm :
NDC Package Code : 66412-0506
Start Marketing Date : 2021-01-05
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
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 : 2016-02-25
Pay. Date : 2016-02-10
DMF Number : 4991
Submission : 1983-05-28
Status : Active
Type : II
Available Reg Filing : CA, ASMF |
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-10-04
Pay. Date : 2013-09-26
DMF Number : 14226
Submission : 1999-06-22
Status : Active
Type : II
Registration Number : 221MF10041
Registrant's Address : NUERNBERGER STRASSE 12, 90537 FEUCHT, GERMANY
Initial Date of Registration : 2009-02-23
Latest Date of Registration : --
NDC Package Code : 46014-1114
Start Marketing Date : 1999-10-22
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 : 24585
Submission : 2011-01-28
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2019-11-18
Pay. Date : 2019-09-25
DMF Number : 33692
Submission : 2019-03-26
Status : Active
Type : II
Certificate Number : R0-CEP 2020-360 - Rev 00
Issue Date : 2023-02-01
Type : Chemical
Substance Number : 616
Status : Valid
Date of Issue : 2020-07-27
Valid Till : 2022-08-08
Written Confirmation Number : WC-0383A6
Address of the Firm :
NDC Package Code : 69766-069
Start Marketing Date : 2019-03-26
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2020-01-21
Pay. Date : 2019-11-14
DMF Number : 34190
Submission : 2019-11-22
Status : Active
Type : II
Certificate Number : CEP 2020-026 - Rev 01
Issue Date : 2024-02-22
Type : Chemical
Substance Number : 616
Status : Valid
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10946
Submission : 1994-06-13
Status : Active
Type : II
Certificate Number : R1-CEP 1998-076 - Rev 09
Issue Date : 2014-06-05
Type : Chemical
Substance Number : 616
Status : Valid
NDC Package Code : 12578-617
Start Marketing Date : 1989-02-08
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 : 7486
Submission : 1988-05-17
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 23311
Submission : 2009-11-20
Status : Inactive
Type : II
Certificate Number : R1-CEP 2003-206 - Rev 03
Issue Date : 2019-07-01
Type : Chemical
Substance Number : 616
Status : Valid
Date of Issue : 2022-06-03
Valid Till : 2025-07-28
Written Confirmation Number : WC-0056
Address of the Firm :
Registrant Name : Pharmapia Co., Ltd.
Registration Date : 2021-03-09
Registration Number : 20210309-209-J-600
Manufacturer Name : RPG Life Sciences Limited
Manufacturer Address : 25, MIDC Land Thane-Belapur Road, Navi Mumbai - 400 703, INDIA
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6200
Submission : 1986-02-12
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7157
Submission : 1987-09-25
Status : Inactive
Type : II
Registration Number : 219MF10333
Registrant's Address : Piazzale Luigi Cadorna, 4 - 20123 MILANO, Italy
Initial Date of Registration : 2007-11-20
Latest Date of Registration : --
NDC Package Code : 48292-0007
Start Marketing Date : 2015-02-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
Certificate Number : R0-CEP 2000-179 - Rev 01
Issue Date : 2002-03-12
Type : Chemical
Substance Number : 616
Status : Withdrawn by Holder
NDC Package Code : 12578-617
Start Marketing Date : 1989-02-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0518
Start Marketing Date : 2018-11-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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 : 5364
Submission : 1984-04-27
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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 : 6800
Submission : 1987-02-02
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
A Haloperidol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Haloperidol, including repackagers and relabelers. The FDA regulates Haloperidol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Haloperidol 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 Haloperidol supplier is an individual or a company that provides Haloperidol active pharmaceutical ingredient (API) or Haloperidol finished formulations upon request. The Haloperidol suppliers may include Haloperidol API manufacturers, exporters, distributors and traders.
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