Veranova: A CDMO that manages complexity with confidence.
01 2Veranova
02 1SCI Pharmtech
03 1Cohance Lifesciences
04 1Malladi Drugs & Pharmaceuticals Limited
05 1HRV Global Life Sciences
06 3Noramco
07 1Tenatra Chemie
08 1Alkem Laboratories
09 1American Pacific Corporation
10 1Boehringer Ingelheim GmbH
11 1Cambrex Corporation
12 1Centaur Pharmaceuticals
13 1Chattem Chemicals, Inc
14 1Cody Laboratories, Inc.
15 1Curia
16 1Dishman Carbogen Amcis
17 2Harman Finochem
18 1Ipca Laboratories
19 2Johnson & Johnson Innovative Medicine
20 2Mallinckrodt Pharmaceuticals
21 1Novartis Pharmaceuticals Corporation
22 1Pellets Pharma Limited
23 1Resonance Laboratories Pvt. Ltd
24 1Rubio Laboratories
25 1Siegfried AG
26 2Sriam Labs
27 1Sun Pharmaceutical Industries Limited
28 1Synergene Active Ingredients Pvt Ltd
29 1UCB Pharma S.A
01 1Belgium
02 1Germany
03 16India
04 2Ireland
05 1Spain
06 2Switzerland
07 1Taiwan
08 12U.S.A
01 14Active
02 6Inactive
03 16Blank
01 15Valid
02 1Withdrawn by Holder
03 20Blank
01 1302MF10009
02 35Blank
01 1WC-0045nA2
02 1WC-0091
03 1WC-0168
04 1WC-0195
05 1WC-0228
06 1WC-288
07 30Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10137
Submission : 1993-03-05
Status : Active
Type : II
Certificate Number : CEP 2017-119 - Rev 01
Issue Date : 2024-10-14
Type : Chemical
Substance Number : 2235
Status : Valid
Registration Number : 302MF10009
Registrant's Address : 10 Wheatfield Road, Edinburgh EH11 2QA, United Kingdom
Initial Date of Registration : 2020-01-17
Latest Date of Registration : --
NDC Package Code : 49812-0020
Start Marketing Date : 2010-06-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Hwanin Pharmaceutical Co., Ltd.
Registration Date : 2021-12-17
Registration Number : 20210427-209-J-837(1)
Manufacturer Name : Macfarlan Smith Limited@Macfarlan Smith Limited
Manufacturer Address : 10 Wheatfield Road, Edinburgh, EH11 2QA, United Kingdom@Three Trees Road, Newbie, Annan, DG12 5QH, United Kingdom
Available Reg Filing : ROW |
SCI Pharmtech offers high-quality, cost-effective APIs, advanced intermediates, & custom products with global expertise and precision.
Certificate Number : R1-CEP 2012-168 - Rev 01
Issue Date : 2022-09-09
Type : Chemical
Substance Number : 2235
Status : Valid
Registrant Name : Aging Life Science Co., Ltd.
Registration Date : 2018-09-07
Registration Number : 20180907-209-J-55
Manufacturer Name : SCI Pharmtech, Inc
Manufacturer Address : No.61, Ln.309, Haihu N. Rd., Luzhu Dist. Taoyuan City 33856, Taiwan
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Certificate Number : CEP 2017-181 - Rev 02
Issue Date : 2024-12-05
Type : Chemical
Substance Number : 2235
Status : Valid
Date of Issue : 2022-08-25
Valid Till : 2025-07-02
Written Confirmation Number : WC-0195
Address of the Firm :
Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
Noramco is a partner to the pharmaceutical industry for controlled substance development & manufacturing.
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-03-27
Pay. Date : 2012-11-23
DMF Number : 22244
Submission : 2008-12-19
Status : Active
Type : II
Certificate Number : CEP 2018-030 - Rev 04
Issue Date : 2024-09-26
Type : Chemical
Substance Number : 2235
Status : Valid
NDC Package Code : 51634-0114
Start Marketing Date : 2017-07-31
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-01-31
Pay. Date : 2013-01-07
DMF Number : 19547
Submission : 2006-06-26
Status : Active
Type : II
Certificate Number : R1-CEP 2009-078 - Rev 00
Issue Date : 2015-01-27
Type : Chemical
Substance Number : 2235
Status : Valid
NDC Package Code : 49812-0020
Start Marketing Date : 2010-06-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Hwanin Pharmaceutical Co., Ltd.
Registration Date : 2021-12-17
Registration Number : 20210427-209-J-837(1)
Manufacturer Name : Macfarlan Smith Limited@Macfarlan Smith Limited
Manufacturer Address : 10 Wheatfield Road, Edinburgh, EH11 2QA, United Kingdom@Three Trees Road, Newbie, Annan, DG12 5QH, United Kingdom
Available Reg Filing : ROW |
Noramco is a partner to the pharmaceutical industry for controlled substance development & manufacturing.
GDUFA
DMF Review : Reviewed
Rev. Date : 2014-07-07
Pay. Date : 2013-07-19
DMF Number : 27208
Submission : 2013-07-12
Status : Active
Type : II
NDC Package Code : 51634-0114
Start Marketing Date : 2017-07-31
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Noramco is a partner to the pharmaceutical industry for controlled substance development & manufacturing.
GDUFA
DMF Review : Reviewed
Rev. Date : 2016-09-19
Pay. Date : 2015-09-15
DMF Number : 29411
Submission : 2016-05-27
Status : Active
Type : II
NDC Package Code : 51634-0114
Start Marketing Date : 2017-07-31
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 : 30116
Submission : 2016-04-14
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-02-08
Pay. Date : 2012-11-27
DMF Number : 12769
Submission : 1997-11-25
Status : Active
Type : II
Certificate Number : CEP 2020-005 - Rev 01
Issue Date : 2024-10-17
Type : Chemical
Substance Number : 2235
Status : Valid
NDC Package Code : 0406-0570
Start Marketing Date : 2014-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Korea Pharma Co., Ltd.
Registration Date : 2023-10-26
Registration Number : 20231012-209-J-1551(A)
Manufacturer Name : SpecGx LLC
Manufacturer Address : 3600 North Second Street, St, Louis, Missouri 63147, USA
GDUFA
DMF Review : Reviewed
Rev. Date : 2014-05-05
Pay. Date : 2013-11-25
DMF Number : 25776
Submission : 2013-09-30
Status : Active
Type : II
Certificate Number : R1-CEP 2009-140 - Rev 01
Issue Date : 2018-02-06
Type : Chemical
Substance Number : 2235
Status : Valid
NDC Package Code : 0406-0570
Start Marketing Date : 2014-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Korea Pharma Co., Ltd.
Registration Date : 2023-10-26
Registration Number : 20231012-209-J-1551(A)
Manufacturer Name : SpecGx LLC
Manufacturer Address : 3600 North Second Street, St, Louis, Missouri 63147, USA
GDUFA
DMF Review : Reviewed
Rev. Date : 2012-11-04
Pay. Date : 2012-11-16
DMF Number : 16331
Submission : 2002-12-20
Status : Active
Type : II
NDC Package Code : 61960-7000
Start Marketing Date : 2002-09-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2012-11-04
Pay. Date : 2012-11-14
DMF Number : 19063
Submission : 2005-12-23
Status : Active
Type : II
NDC Package Code : 17180-1724
Start Marketing Date : 2012-06-26
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 : 16610
Submission : 2003-05-20
Status : Active
Type : II
NDC Package Code : 59116-3390
Start Marketing Date : 2012-10-26
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2016-10-30
Pay. Date : 2016-08-03
DMF Number : 30682
Submission : 2016-07-29
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 30510
Submission : 2016-05-25
Status : Active
Type : II
Certificate Number : CEP 2009-219 - Rev 04
Issue Date : 2024-12-23
Type : Chemical
Substance Number : 2235
Status : Valid
NDC Package Code : 65267-114
Start Marketing Date : 2008-12-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Korea Janssen Co., Ltd.
Registration Date : 2020-07-15
Registration Number : 20200715-209-J-691
Manufacturer Name : Janssen Pharmaceuticals, Inc
Manufacturer Address : 1440 Olympic Drive, Athens, Georgia (GA) 30601, USA
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 30546
Submission : 2021-07-30
Status : Active
Type : II
NDC Package Code : 65267-114
Start Marketing Date : 2008-12-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Korea Janssen Co., Ltd.
Registration Date : 2020-07-15
Registration Number : 20200715-209-J-691
Manufacturer Name : Janssen Pharmaceuticals, Inc
Manufacturer Address : 1440 Olympic Drive, Athens, Georgia (GA) 30601, USA
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 33509
Submission : 2019-03-12
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 20621
Submission : 2007-07-05
Status : Inactive
Type : II
Certificate Number : R1-CEP 2009-094 - Rev 00
Issue Date : 2015-08-03
Type : Chemical
Substance Number : 2235
Status : Valid
Date of Issue : 2022-06-08
Valid Till : 2025-07-02
Written Confirmation Number : WC-0091
Address of the Firm :
Registrant Name : Myungin Pharmaceutical Co., Ltd.
Registration Date : 2021-04-16
Registration Number : 20210416-209-J-940
Manufacturer Name : IPCA Laboratories Limited
Manufacturer Address : PO Sejavta Dist. Ratlam (MP) - 457 001, India
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 : 4599
Submission : 1982-06-16
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 12989
Submission : 1998-05-15
Status : Inactive
Type : II
Certificate Number : R1-CEP 2011-378 - Rev 01
Issue Date : 2018-10-19
Type : Chemical
Substance Number : 2235
Status : Valid
NDC Package Code : 0792-0101
Start Marketing Date : 2019-12-18
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 : 11635
Submission : 1995-08-31
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15485
Submission : 2001-06-20
Status : Inactive
Type : II
Certificate Number : R1-CEP 2009-254 - Rev 00
Issue Date : 2015-11-25
Type : Chemical
Substance Number : 2235
Status : Withdrawn by Holder
Certificate Number : CEP 2009-359 - Rev 02
Issue Date : 2024-03-05
Type : Chemical
Substance Number : 2235
Status : Valid
Date of Issue : 2022-08-08
Valid Till : 2025-07-14
Written Confirmation Number : WC-0168
Address of the Firm :
Certificate Number : R1-CEP 2016-073 - Rev 00
Issue Date : 2022-03-08
Type : Chemical
Substance Number : 2235
Status : Valid
Certificate Number : R1-CEP 2010-031 - Rev 02
Issue Date : 2022-04-08
Type : Chemical
Substance Number : 2235
Status : Valid
Date of Issue : 2022-06-08
Valid Till : 2025-07-21
Written Confirmation Number : WC-0045nA2
Address of the Firm :
Registrant Name : Alvogen Korea Co., Ltd.
Registration Date : 2023-07-31
Registration Number : 20230731-209-J-1530
Manufacturer Name : Harman Finochem Limited
Manufacturer Address : Plot No. E-7, E-8, E-9, MIDC Industrial area, Chikalthana, Aurangabad-431 006, Maharastra, India
Certificate Number : R0-CEP 2021-474 - Rev 00
Issue Date : 2022-05-25
Type : Chemical
Substance Number : 2235
Status : Valid
Registrant Name : Alvogen Korea Co., Ltd.
Registration Date : 2023-07-31
Registration Number : 20230731-209-J-1530
Manufacturer Name : Harman Finochem Limited
Manufacturer Address : Plot No. E-7, E-8, E-9, MIDC Industrial area, Chikalthana, Aurangabad-431 006, Maharastra, India
Certificate Number : CEP 2021-119 - Rev 02
Issue Date : 2024-11-12
Type : Chemical
Substance Number : 2235
Status : Valid
A Methylphenidate Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Methylphenidate Hydrochloride, including repackagers and relabelers. The FDA regulates Methylphenidate Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Methylphenidate 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 Methylphenidate Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Methylphenidate Hydrochloride supplier is an individual or a company that provides Methylphenidate Hydrochloride active pharmaceutical ingredient (API) or Methylphenidate Hydrochloride finished formulations upon request. The Methylphenidate Hydrochloride suppliers may include Methylphenidate Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Methylphenidate Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
We have 29 companies offering Methylphenidate Hydrochloride
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