Minakem is manufacturing small molecules APIs including corticosteroids
01 2DELMAR CHEMICALS INC
02 1Emcure Pharmaceuticals Limited
01 2PENTAMIDINE ISETHIONATE
02 1Pentamidine Isethionate
01 2Canada
02 1India
Minakem is manufacturing small molecules APIs including corticosteroids
NDC Package Code : 11712-788
Start Marketing Date : 1986-07-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Minakem is manufacturing small molecules APIs including corticosteroids
NDC Package Code : 11712-790
Start Marketing Date : 1986-07-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14593-930
Start Marketing Date : 2022-02-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (15kg/15kg)
Marketing Category : BULK INGREDIENT
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A Pentacarinat manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pentacarinat, including repackagers and relabelers. The FDA regulates Pentacarinat manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pentacarinat 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 Pentacarinat supplier is an individual or a company that provides Pentacarinat active pharmaceutical ingredient (API) or Pentacarinat finished formulations upon request. The Pentacarinat suppliers may include Pentacarinat API manufacturers, exporters, distributors and traders.
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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 Pentacarinat as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Pentacarinat 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 Pentacarinat 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 Pentacarinat and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Pentacarinat NDC to their finished compounded human drug products, they may choose to do so.
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