LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.

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01 1LGM Pharma
02 1Jai Radhe Sales
03 1Tenatra Exports
04 1Zeal Medipharma
05 1Cosma (C.F.M. Group)
06 1Amsa
07 1Anphar Laboratories
08 1Arch Pharmalabs
09 1Benzo Chem Industries Pvt
10 1Emcure Pharmaceuticals
11 2Fagron Group
12 1Guangzhou Tosun Pharmaceutical
13 1H. Lundbeck AS
14 1Icrom
15 2Ipca Laboratories
16 1Liaoyuan Silver Eagle Pharmaceutical
17 1Osmopharm
18 1Pcca
19 1Suvan Lifesciences
20 1Suzhou Ryway Biotech
21 1Waitaki Biosciences
22 2Blank
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01 3China
02 1Denmark
03 10India
04 3Italy
05 2Netherlands
06 1New Zealand
07 1Switzerland
08 1U.S.A
09 1United Kingdom
10 2Blank
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01 6Active
02 3Inactive
03 16Blank
01 4Valid
02 21Blank
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01 1221MF10057
02 24Blank
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01 1WC-0091
02 1WC-0258n
03 1WC-0583
04 22Blank
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01 25Blank
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01 140700-0010
02 145562-1737
03 151552-1549
04 151604-0005
05 151927-0185
06 151927-1082
07 157451-1119
08 157451-1139
09 176003-0739
10 16Blank
01 25Blank
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.
Delivering Quality APIs, Drug Intermediates, and Specialty Chemicals to Over 50 Countries Across the Globe.
Cosma S.p.A., part of CFM Group with AMSA & Clarochem, provides global pharma & veterinary health with 300+ tons of FDA-approved APIs.
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 : 2026-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
| Available Reg Filing : ASMF |
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 :
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 : 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 : 2025-06-19
Valid Till : 2028-07-02
Written Confirmation Number : WC-0091
Address of the Firm :
NDC Package Code : 57451-1119
Start Marketing Date : 2012-06-02
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 21271
Submission : 2008-01-22
Status : Inactive
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5023
Submission : 1983-07-25
Status : Inactive
Type : II

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PharmaCompass offers a list of Metoclopramide Hydrochloride 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 Metoclopramide Hydrochloride manufacturer or Metoclopramide Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Metoclopramide Hydrochloride API Price utilized in the formulation of products. Metoclopramide Hydrochloride API Price is not always fixed or binding as the Metoclopramide Hydrochloride Price is obtained through a variety of data sources. The Metoclopramide Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Primperan (tablet) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Primperan (tablet), including repackagers and relabelers. The FDA regulates Primperan (tablet) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Primperan (tablet) 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 Primperan (tablet) manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Primperan (tablet) supplier is an individual or a company that provides Primperan (tablet) active pharmaceutical ingredient (API) or Primperan (tablet) finished formulations upon request. The Primperan (tablet) suppliers may include Primperan (tablet) API manufacturers, exporters, distributors and traders.
click here to find a list of Primperan (tablet) suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
We have 21 companies offering Primperan (tablet)
Get in contact with the supplier of your choice: