Curia - Accelerating therapies from discovery to commercialization with flexible, scalable CDMO solutions.
01 1Curia
02 1Apicore
03 1Matrix Pharmaceutical Inc
04 1Par Pharmaceutical
05 1Shouyuan Chemical
06 2Viatris
07 1Vintage Pharmaceuticals-Charlotte
08 1Blank
01 1China
02 1India
03 6U.S.A
04 1Blank
01 4Active
02 5Blank
01 9Blank
01 9Blank
01 9Blank
01 9Blank
01 142973-157
02 165392-2801
03 170054-021
04 184206-0062
05 5Blank
01 9Blank
Curia - Accelerating therapies from discovery to commercialization with flexible, scalable CDMO solutions.
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GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 12419
Submission : 1997-03-17
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 24722
Submission : 2011-03-08
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2014-06-23
Pay. Date : 2013-12-19
DMF Number : 24615
Submission : 2011-05-03
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 32292
Submission : 2017-12-19
Status : Active
Type : II
NDC Package Code : 84206-0062
Start Marketing Date : 2024-10-10
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
NDC Package Code : 65392-2801
Start Marketing Date : 1998-06-05
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
NDC Package Code : 70054-021
Start Marketing Date : 2018-12-17
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (5kg/5kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 42973-157
Start Marketing Date : 2010-06-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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A Sulfamylon manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sulfamylon, including repackagers and relabelers. The FDA regulates Sulfamylon manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sulfamylon 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 Sulfamylon supplier is an individual or a company that provides Sulfamylon active pharmaceutical ingredient (API) or Sulfamylon finished formulations upon request. The Sulfamylon suppliers may include Sulfamylon API manufacturers, exporters, distributors and traders.
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