Minakem is manufacturing small molecules APIs including corticosteroids
01 4DELMAR CHEMICALS INC
02 2Biocon Limited
03 1F.I.S. FABBRICA ITALIANA SINTETICI S.P.A.
04 1MSN Laboratories Private Limited
01 1FLUVASTATIN SODIUM
02 1FLUVASTATIN SODIUM HYDRATE milled
03 1FLUVASTATIN SODIUM HYDRATE unmilled
04 1FLUVASTATIN SODIUM milled
05 1FLUVASTATIN SODIUM unmilled
06 2Fluvastatin Sodium
07 1Fluvastatin sodium Amorphous
01 4Canada
02 3India
03 1Italy
Minakem is manufacturing small molecules APIs including corticosteroids
NDC Package Code : 11712-396
Start Marketing Date : 2002-08-14
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Minakem is manufacturing small molecules APIs including corticosteroids
NDC Package Code : 11712-397
Start Marketing Date : 2002-08-14
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Minakem is manufacturing small molecules APIs including corticosteroids
NDC Package Code : 11712-398
Start Marketing Date : 2002-08-14
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Minakem is manufacturing small molecules APIs including corticosteroids
NDC Package Code : 11712-399
Start Marketing Date : 2002-08-14
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65727-012
Start Marketing Date : 2007-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65727-017
Start Marketing Date : 2007-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 48087-0093
Start Marketing Date : 2010-11-29
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14501-0009
Start Marketing Date : 2010-03-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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A AKOS016340657 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AKOS016340657, including repackagers and relabelers. The FDA regulates AKOS016340657 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AKOS016340657 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 AKOS016340657 supplier is an individual or a company that provides AKOS016340657 active pharmaceutical ingredient (API) or AKOS016340657 finished formulations upon request. The AKOS016340657 suppliers may include AKOS016340657 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 AKOS016340657 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for AKOS016340657 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 AKOS016340657 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 AKOS016340657 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a AKOS016340657 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of AKOS016340657 suppliers with NDC on PharmaCompass.
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