Atman Pharmaceuticals: A One Stop Solution Provider to All Your API Needs.
01 1Atman Pharmaceuticals
02 1LGM Pharma
03 1Jai Radhe Sales
04 1Tenatra Chemie
05 1Amsa Spa
06 1Anphar Laboratories
07 1Arch Pharmalabs
08 1Benzo Chem Industries Pvt
09 1COSMA S.p.A
10 1Emcure Pharmaceuticals
11 1Guangzhou Tosun Pharmaceutical
12 1H. Lundbeck AS
13 1Heumann
14 1Icrom
15 1Ipca Laboratories
16 1Liaoyuan Silver Eagle Pharmaceutical
17 1Osmopharm
18 1Suvan Lifesciences
19 1Suzhou Ryway Biotech
20 1Waitaki Biosciences
21 1Blank
01 3China
02 1Denmark
03 1Germany
04 9India
05 3Italy
06 1New Zealand
07 1Switzerland
08 1U.S.A
09 1Blank
01 6Active
02 4Inactive
03 11Blank
01 4Valid
02 17Blank
01 1221MF10057
02 20Blank
01 1WC-0091
02 1WC-0226
03 1WC-258
04 18Blank
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 28987
Submission : 2014-12-18
Status : Active
Type : II
Certificate Number : CEP 2015-082 - Rev 01
Issue Date : 2024-03-08
Type : Chemical
Substance Number : 674
Status : Valid
GDUFA
DMF Review : Reviewed
Rev. Date : 2018-09-10
Pay. Date : 2018-08-06
DMF Number : 32991
Submission : 2018-08-03
Status : Active
Type : II
Date of Issue : 2019-10-07
Valid Till : 2022-07-02
Written Confirmation Number : WC-0226
Address of the Firm :
GDUFA
DMF Review : Reviewed
Rev. Date : 2016-07-28
Pay. Date : 2016-07-21
DMF Number : 4877
Submission : 1983-03-26
Status : Active
Type : II
NDC Package Code : 45562-1737
Start Marketing Date : 1998-01-07
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-01-11
Pay. Date : 2012-12-10
DMF Number : 7581
Submission : 1988-07-15
Status : Active
Type : II
Certificate Number : CEP 2004-075 - Rev 05
Issue Date : 2024-03-12
Type : Chemical
Substance Number : 674
Status : Valid
Date of Issue : 2022-06-08
Valid Till : 2025-07-02
Written Confirmation Number : WC-0091
Address of the Firm :
NDC Package Code : 57451-1119
Start Marketing Date : 2012-06-02
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2018-03-02
Pay. Date : 2018-01-12
DMF Number : 4523
Submission : 1982-05-03
Status : Active
Type : II
NDC Package Code : 51604-0005
Start Marketing Date : 2009-10-14
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2019-01-29
Pay. Date : 2018-07-24
DMF Number : 32884
Submission : 2018-06-19
Status : Active
Type : II
Certificate Number : R1-CEP 2015-304 - Rev 00
Issue Date : 2021-05-20
Type : Chemical
Substance Number : 674
Status : Valid
NDC Package Code : 40700-0010
Start Marketing Date : 2020-02-20
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 : 5756
Submission : 1985-03-29
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5023
Submission : 1983-07-25
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 21271
Submission : 2008-01-22
Status : Inactive
Type : II
Date of Issue : 2013-12-19
Valid Till : 2016-11-21
Written Confirmation Number : WC-258
Address of the Firm :
Certificate Number : CEP 2023-100 - Rev 00
Issue Date : 2024-03-28
Type : Chemical
Substance Number : 674
Status : Valid
Registration Number : 221MF10057
Registrant's Address : VIALE DEL GHISALLO, 20 20151 MILAN ITALY
Initial Date of Registration : 2009-03-19
Latest Date of Registration : --
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 : 4381
Submission : 1981-09-14
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
A Metoclopramide Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Metoclopramide Hydrochloride, including repackagers and relabelers. The FDA regulates Metoclopramide Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Metoclopramide 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 Metoclopramide Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Metoclopramide Hydrochloride supplier is an individual or a company that provides Metoclopramide Hydrochloride active pharmaceutical ingredient (API) or Metoclopramide Hydrochloride finished formulations upon request. The Metoclopramide Hydrochloride suppliers may include Metoclopramide Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Metoclopramide Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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