Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
01 1Symbiotec Pharmalab Private Limited
02 1Farmabios S.p.A.
03 1Curia Spain S.A.U.
04 1LETCO MEDICAL, LLC
05 1Medisca Inc.
06 1NEWCHEM SPA
07 1Professional Compounding Centers of America
08 1Professional Compounding Centers of America dba PCCA
09 1SYMBIOTICA SPECIALITY INGREDIENTS SDN.BHD
10 1Sicor S.r.l.
11 1Spectrum Laboratory Products, Inc.
01 3BETAMETHASONE DIPROPIONATE
02 1BETAMETHASONE DIPROPIONATE MICRONIZED
03 3Betamethasone Dipropionate
04 1Betamethasone Dipropionate Micr
05 1Betamethasone Dipropionate Micro
06 1Betamethasone Dipropionate Micronized
07 1Betamethasone dipropionate
01 1Germany
02 1India
03 2Italy
04 1Malaysia
05 4U.S.A
06 2United Kingdom
Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
NDC Package Code : 22552-0028
Start Marketing Date : 2011-08-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Axplora- The partner of choice for complex APIs.
NDC Package Code : 46439-8710
Start Marketing Date : 1989-05-31
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62991-1023
Start Marketing Date : 2011-05-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 38779-0017
Start Marketing Date : 2015-07-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 24002-0019
Start Marketing Date : 2009-08-03
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0171
Start Marketing Date : 2011-10-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-1454
Start Marketing Date : 2013-06-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 53183-0433
Start Marketing Date : 2017-11-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-1075
Start Marketing Date : 1989-04-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 52128-160
Start Marketing Date : 2011-11-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Betamethasone Dipropionate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Betamethasone Dipropionate, including repackagers and relabelers. The FDA regulates Betamethasone Dipropionate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Betamethasone Dipropionate 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 Dipropionate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Betamethasone Dipropionate supplier is an individual or a company that provides Betamethasone Dipropionate active pharmaceutical ingredient (API) or Betamethasone Dipropionate finished formulations upon request. The Betamethasone Dipropionate suppliers may include Betamethasone Dipropionate API manufacturers, exporters, distributors and traders.
click here to find a list of Betamethasone Dipropionate 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 Dipropionate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Betamethasone Dipropionate 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 Dipropionate 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 Dipropionate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Betamethasone Dipropionate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Betamethasone Dipropionate suppliers with NDC on PharmaCompass.
We have 10 companies offering Betamethasone Dipropionate
Get in contact with the supplier of your choice:
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