Curia - Accelerating therapies from discovery to commercialization with flexible, scalable CDMO solutions.

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01 1Curia
02 1Cerata Pharmaceuticals LLP
03 1Symbiotec Pharmalab
04 1Pfizer CentreOne
05 2EUROAPI
06 1Bioquim
07 2Symbiotica Speciality Ingredients Sdn Bhd
08 1Henan Lihua Pharmaceutical
09 1Lupin Ltd
10 1Taro Pharmaceutical Industries
11 1Trifarma
12 1Yangzhou Pharmaceutical
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01 2China
02 2France
03 3India
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07 3U.S.A
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01 13923/25
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01 252128-136
02 164958-0080
03 182298-115
04 182298-116
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Curia - Accelerating therapies from discovery to commercialization with flexible, scalable CDMO solutions.
Cerata Pharmaceuticals LLP: WHO-GMP Certified Leading Manufacturer & Exporter of Steroid-Hormone & Peptide APIs From India.
NDC Package Code : 82298-115
Start Marketing Date : 2011-02-07
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Bioquim: An European GMP-certified company manufacturing bulk APIs, specializing in sterile lyophilization and chemical synthesis.
Symbiotica delivers high-quality APIs through advanced R&D, GMP-certified manufacturing, & trusted global pharmaceutical partnerships.
GDUFA
DMF Review : Reviewed
Rev. Date : 2017-11-07
Pay. Date : 2017-06-05
DMF Number : 31423
Submission : 2017-02-01
Status : Active
Type : II
Date of Issue : 2025-05-20
Valid Till : 2028-05-22
Written Confirmation Number : 3923/25
Address of the Firm :
NDC Package Code : 52128-136
Start Marketing Date : 2011-03-10
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (10kg/10kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 82298-116
Start Marketing Date : 2011-02-07
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Symbiotica delivers high-quality APIs through advanced R&D, GMP-certified manufacturing, & trusted global pharmaceutical partnerships.
NDC Package Code : 52128-136
Start Marketing Date : 2007-08-09
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2019-10-07
Pay. Date : 2019-04-29
DMF Number : 33334
Submission : 2018-12-19
Status : Active
Type : II

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PharmaCompass offers a list of Hydrocortisone Valerate 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 Hydrocortisone Valerate manufacturer or Hydrocortisone Valerate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Hydrocortisone Valerate manufacturer or Hydrocortisone Valerate supplier.
A Hydrocortisone Valerate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hydrocortisone Valerate, including repackagers and relabelers. The FDA regulates Hydrocortisone Valerate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hydrocortisone Valerate 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 Hydrocortisone Valerate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Hydrocortisone Valerate supplier is an individual or a company that provides Hydrocortisone Valerate active pharmaceutical ingredient (API) or Hydrocortisone Valerate finished formulations upon request. The Hydrocortisone Valerate suppliers may include Hydrocortisone Valerate API manufacturers, exporters, distributors and traders.
click here to find a list of Hydrocortisone Valerate suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
We have 12 companies offering Hydrocortisone Valerate
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