Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
01 1Symbiotec Pharmalab Private Limited
02 1Curia Spain SAU
03 1Hovione FarmaCiencia SA
04 1NEWCHEM SPA
05 1Professional Compounding Centers of America
06 1SYMBIOTICA SPECIALITY INGREDIENTS SDN.BHD
07 2Sicor S.r.l.
01 1BETAMETHASONE
02 2BETAMETHASONE ACETATE MICRONIZED
03 4Betamethasone Acetate
04 1Betamethasone Acetate Micronized
01 1India
02 3Italy
03 1Malaysia
04 1Portugal
05 1U.S.A
06 1United Kingdom
Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
NDC Package Code : 22552-0041
Start Marketing Date : 2014-12-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65089-0006
Start Marketing Date : 2024-04-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50909-5103
Start Marketing Date : 1986-11-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 24002-0026
Start Marketing Date : 2002-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0278
Start Marketing Date : 2013-06-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 53183-0459
Start Marketing Date : 2019-08-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53183-2459
Start Marketing Date : 2016-04-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 52128-166
Start Marketing Date : 2013-03-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Betamethasone Acetate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Betamethasone Acetate manufacturer or Betamethasone Acetate supplier for your needs.
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A CELESTONE SOLUSPAN manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CELESTONE SOLUSPAN, including repackagers and relabelers. The FDA regulates CELESTONE SOLUSPAN manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CELESTONE SOLUSPAN 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 CELESTONE SOLUSPAN manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A CELESTONE SOLUSPAN supplier is an individual or a company that provides CELESTONE SOLUSPAN active pharmaceutical ingredient (API) or CELESTONE SOLUSPAN finished formulations upon request. The CELESTONE SOLUSPAN suppliers may include CELESTONE SOLUSPAN API manufacturers, exporters, distributors and traders.
click here to find a list of CELESTONE SOLUSPAN suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price 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 CELESTONE SOLUSPAN as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for CELESTONE SOLUSPAN 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 CELESTONE SOLUSPAN 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 CELESTONE SOLUSPAN and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a CELESTONE SOLUSPAN NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of CELESTONE SOLUSPAN suppliers with NDC on PharmaCompass.
We have 7 companies offering CELESTONE SOLUSPAN
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