Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1Coprima SL
02 1Moehs Catalana SL
03 1COSMA Spa
04 1DARMERICA, LLC
05 1Holiday Labs Mexico, S.A. De C.V.
06 3Ipca Laboratories Limited
07 1KALCHEM INTERNATIONAL INC
08 1LETCO MEDICAL, LLC
09 1MINSHENG GROUP SHAOXING PHARMACEUTICAL CO., LTD.
10 1Medisca Inc.
11 1Megafine Pharma (P) Limited
12 1Professional Compounding Centers of America
01 4PYRANTEL PAMOATE
02 10Pyrantel Pamoate
01 1China
02 4India
03 1Italy
04 2Spain
05 4U.S.A
06 1United Kingdom
07 1Blank
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
NDC Package Code : 52932-0714
Start Marketing Date : 2009-09-29
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Cosma S.p.A., part of CFM Group with AMSA & Clarochem, provides global pharma & veterinary health with 300+ tons of FDA-approved APIs.
NDC Package Code : 51604-0013
Start Marketing Date : 2009-10-14
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
NDC Package Code : 68294-0008
Start Marketing Date : 2021-01-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 57451-1113
Start Marketing Date : 2012-03-26
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 57451-0004
Start Marketing Date : 2012-04-12
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0059
Start Marketing Date : 2014-06-17
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 22665-0002
Start Marketing Date : 2010-07-19
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 13371-414
Start Marketing Date : 2014-05-14
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0235
Start Marketing Date : 2022-03-04
End Marketing Date : 2027-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 52286-0019
Start Marketing Date : 2009-11-04
End Marketing Date : 2027-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Pyrantel Pamoate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Pyrantel Pamoate manufacturer or Pyrantel Pamoate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pyrantel Pamoate manufacturer or Pyrantel Pamoate supplier.
A Helmintox manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Helmintox, including repackagers and relabelers. The FDA regulates Helmintox manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Helmintox 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 Helmintox manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Helmintox supplier is an individual or a company that provides Helmintox active pharmaceutical ingredient (API) or Helmintox finished formulations upon request. The Helmintox suppliers may include Helmintox API manufacturers, exporters, distributors and traders.
click here to find a list of Helmintox suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Helmintox as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Helmintox API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Helmintox as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Helmintox and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Helmintox NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Helmintox suppliers with NDC on PharmaCompass.
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