Axplora- The partner of choice for complex APIs.
01 2Farmabios S.p.A.
02 1Symbiotec Pharmalab Private Limited
03 1Amphastar Nanjing Pharmaceuticals, Inc.
04 1Cipla Ltd.
05 1Curia Spain S.A.U
06 1Industriale Chimica s.r.l.
07 1Medisca Inc.
08 1Professional Compounding Centers of America dba PCCA
09 1SYMBIOTICA SPECIALITY INGREDIENTS SDN.BHD
10 1Sicor S.p.a.
11 1Sicor S.r.l.
12 1Spectrum Laboratory Products, Inc.
01 3BECLOMETHASONE DIPROPIONATE
02 1BECLOMETHASONE DIPROPIONATE ANHYDROUS MICRONIZED
03 1BECLOMETHASONE DIPROPIONATE MONOHYDRATE
04 1Beclometasone Dipropionate Anhydrous
05 5Beclomethasone Dipropionate
06 1Beclomethasone Dipropionate Anhydrous Micronized W.S
07 1Beclomethasone dipropionate
01 2Germany
02 2India
03 3Italy
04 1Malaysia
05 4U.S.A
06 1United Kingdom
NDC Package Code : 46439-8714
Start Marketing Date : 1993-06-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 22552-0038
Start Marketing Date : 2014-01-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
BECLOMETHASONE DIPROPIONATE MONOHYDRATE
NDC Package Code : 46439-8748
Start Marketing Date : 2000-10-09
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 52221-105
Start Marketing Date : 2013-12-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER, FOR SUSPENSION (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53104-7632
Start Marketing Date : 2016-01-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0364
Start Marketing Date : 2015-08-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-1641
Start Marketing Date : 2013-06-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 53183-0407
Start Marketing Date : 2010-07-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-0802
Start Marketing Date : 1997-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 52128-167
Start Marketing Date : 2013-03-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Beclomethasone Dipropionate Monohydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Beclomethasone Dipropionate Monohydrate, including repackagers and relabelers. The FDA regulates Beclomethasone Dipropionate Monohydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Beclomethasone Dipropionate Monohydrate 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 Beclomethasone Dipropionate Monohydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Beclomethasone Dipropionate Monohydrate supplier is an individual or a company that provides Beclomethasone Dipropionate Monohydrate active pharmaceutical ingredient (API) or Beclomethasone Dipropionate Monohydrate finished formulations upon request. The Beclomethasone Dipropionate Monohydrate suppliers may include Beclomethasone Dipropionate Monohydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Beclomethasone Dipropionate Monohydrate 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 Beclomethasone Dipropionate Monohydrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Beclomethasone Dipropionate Monohydrate 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 Beclomethasone Dipropionate Monohydrate 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 Beclomethasone Dipropionate Monohydrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Beclomethasone Dipropionate Monohydrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Beclomethasone Dipropionate Monohydrate suppliers with NDC on PharmaCompass.
We have 12 companies offering Beclomethasone Dipropionate Monohydrate
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