Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
01 1Symbiotec Pharmalab Private Limited
02 1Curia Spain S.A.U.
03 1Hovione FarmaCiencia SA
04 1LETCO MEDICAL, LLC
05 1MSD International GmbH (Singapore Branch)
06 1Medisca Inc.
07 1Newchem spa
08 1Professional Compounding Centers of America dba PCCA
09 1SYMBIOTICA SPECIALITY INGREDIENTS SDN.BHD
10 1Spectrum Laboratory Products, Inc.
01 2BETAMETHASONE SODIUM PHOSPHATE
02 6Betamethasone Sodium Phosphate
03 2Betamethasone sodium phosphate
01 1India
02 1Italy
03 1Malaysia
04 1Portugal
05 5U.S.A
06 1United Kingdom
BETAMETHASONE SODIUM PHOSPHATE
NDC Package Code : 22552-0040
Start Marketing Date : 2014-12-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
BETAMETHASONE SODIUM PHOSPHATE
NDC Package Code : 65089-0004
Start Marketing Date : 1965-03-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
BETAMETHASONE SODIUM PHOSPHATE
NDC Package Code : 50909-5102
Start Marketing Date : 1986-11-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
BETAMETHASONE SODIUM PHOSPHATE
NDC Package Code : 62991-1024
Start Marketing Date : 2011-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
BETAMETHASONE SODIUM PHOSPHATE
NDC Package Code : 38779-0195
Start Marketing Date : 2011-05-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
BETAMETHASONE SODIUM PHOSPHATE
NDC Package Code : 75895-0037
Start Marketing Date : 1965-03-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
BETAMETHASONE SODIUM PHOSPHATE
NDC Package Code : 24002-0024
Start Marketing Date : 2012-12-21
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
BETAMETHASONE SODIUM PHOSPHATE
NDC Package Code : 51927-1951
Start Marketing Date : 2013-06-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
BETAMETHASONE SODIUM PHOSPHATE
NDC Package Code : 49452-1077
Start Marketing Date : 1992-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
BETAMETHASONE SODIUM PHOSPHATE
NDC Package Code : 52128-161
Start Marketing Date : 2011-11-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Betamethasone Sodium Phosphate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Betamethasone Sodium Phosphate, including repackagers and relabelers. The FDA regulates Betamethasone Sodium Phosphate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Betamethasone Sodium Phosphate 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 Betamethasone Sodium Phosphate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Betamethasone Sodium Phosphate supplier is an individual or a company that provides Betamethasone Sodium Phosphate active pharmaceutical ingredient (API) or Betamethasone Sodium Phosphate finished formulations upon request. The Betamethasone Sodium Phosphate suppliers may include Betamethasone Sodium Phosphate API manufacturers, exporters, distributors and traders.
click here to find a list of Betamethasone Sodium Phosphate 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 Betamethasone Sodium Phosphate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Betamethasone Sodium Phosphate 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 Betamethasone Sodium Phosphate 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 Betamethasone Sodium Phosphate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Betamethasone Sodium Phosphate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Betamethasone Sodium Phosphate suppliers with NDC on PharmaCompass.
We have 10 companies offering Betamethasone Sodium Phosphate
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?