Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.

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01 2Symbiotec Pharmalab Limited
02 3Coral Drugs Private Limited
03 1SYMBIOTICA SPECIALITY INGREDIENTS SDN.BHD
04 2Farmabios S.p.A.
05 2Wavelength Enterprises LTD
06 1VAMSI LABS LIMITED.
07 2Aarti Pharmalabs Limited
08 1Willow Birch Pharma, Inc.
09 1Curia Spain S.A.U.
10 1AX Pharmaceutical Corp
11 2Cipla Ltd.
12 1Fagron Inc
13 1Henan Lihua Pharmaceutical Co Ltd
14 2Hovione FarmaCiencia SA
15 4Industriale Chimica s.r.l.
16 1LETCO MEDICAL, LLC
17 1Medisca Inc.
18 1NEWCHEM SPA
19 1Professional Compounding Centers of America
20 1Professional Compounding Centers of America dba PCCA
21 1STERLING SPA
22 2Sicor de Mexico S.A. de C.V
23 2Sterling S.p.A.
24 1zhejiang xianju pharmaceutical co., Ltd.
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01 6MOMETASONE FUROATE
02 1MOMETASONE FUROATE MICRONIZED
03 3MOMETASONE FUROATE MONOHYDRATE
04 18Mometasone Furoate
05 7Mometasone Furoate Monohydrate
06 1Mometasone furoate
07 1mometasone furoate
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01 1Canada
02 2China
03 2Germany
04 10India
05 2Israel
06 8Italy
07 1Malaysia
08 2Mexico
09 1Netherlands
10 2Portugal
11 4U.S.A
12 2United Kingdom
NDC Package Code : 22552-0002
Start Marketing Date : 2017-12-12
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49076-5603
Start Marketing Date : 2025-08-08
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 : 52128-163
Start Marketing Date : 2011-11-23
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46439-8733
Start Marketing Date : 2008-12-12
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
MOMETASONE FUROATE MONOHYDRATE
NDC Package Code : 58175-0551
Start Marketing Date : 2009-02-04
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Vamsi Labs is one of the major manufacturers of Anti-asthmatic, Anti-migraine & Anti-psychotic APIs.
MOMETASONE FUROATE MONOHYDRATE
NDC Package Code : 66412-0686
Start Marketing Date : 2025-07-15
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
Aarti Pharmalabs is a partner of choice for pharmaceutical companies for APIs & Intermediates. Largest Indian producer of Caffeine.
NDC Package Code : 15308-0220
Start Marketing Date : 2006-01-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Willow Birch Pharma delivers trusted, high-quality APIs nationwide with unmatched service, compliance, and competitive value.
NDC Package Code : 10695-111
Start Marketing Date : 2020-07-09
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Curia - Accelerating therapies from discovery to commercialization with flexible, scalable CDMO solutions.
NDC Package Code : 65089-0025
Start Marketing Date : 2014-04-25
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
MOMETASONE FUROATE MONOHYDRATE
NDC Package Code : 22552-0021
Start Marketing Date : 2011-05-13
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Mometasone Furoate 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 Mometasone Furoate manufacturer or Mometasone Furoate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Mometasone Furoate manufacturer or Mometasone Furoate supplier.
A 141646-00-6 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 141646-00-6, including repackagers and relabelers. The FDA regulates 141646-00-6 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 141646-00-6 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 141646-00-6 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A 141646-00-6 supplier is an individual or a company that provides 141646-00-6 active pharmaceutical ingredient (API) or 141646-00-6 finished formulations upon request. The 141646-00-6 suppliers may include 141646-00-6 API manufacturers, exporters, distributors and traders.
click here to find a list of 141646-00-6 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 141646-00-6 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for 141646-00-6 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 141646-00-6 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 141646-00-6 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a 141646-00-6 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of 141646-00-6 suppliers with NDC on PharmaCompass.
We have 22 companies offering 141646-00-6
Get in contact with the supplier of your choice: