Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
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01 1Supriya Lifescience Limited
02 1Neuland Laboratories Limited
03 1AstraZeneca AB
04 1Cambrex Profarmaco Milano Srl
05 1Catalent Micron Technologies, Inc.
06 2Cipla Ltd.
07 2Derivados Quimicos
08 1FDC Limited
09 1Glaxo Operations UK Ltd
10 1Kindeva Drug Delivery Limited
11 2Lusochimica SPA
12 2Melody Healthcare Pvt. Ltd.
13 1Professional Compounding Centers of America
14 1Professional Compounding Centers of America dba PCCA
15 4SICOR Societa' Italiana Corticosteroidi s.r.l.
16 1Spectrum Laboratory Products, Inc.
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01 6ALBUTEROL SULFATE
02 1Albuterol Salbutamol base
03 1Albuterol Salbutamol base micro
04 8Albuterol Sulfate
05 1Albuterol Sulfate Micronised Conditioned
06 1Albuterol Sulfate micronized
07 1Albuterol Sulphate
08 1Salbutamol Sulfate
09 1Salbutamol sulfate micronized
10 1albuterol sulfate
11 1salbutamol sulphate
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01 7India
02 6Italy
03 2Spain
04 4U.S.A
05 4United Kingdom
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
NDC Package Code : 61281-3700
Start Marketing Date : 2019-03-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 58032-0002
Start Marketing Date : 2017-11-27
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17228-9600
Start Marketing Date : 2023-03-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (15kg/15kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12828-0063
Start Marketing Date : 1986-05-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 11517-012
Start Marketing Date : 2015-04-30
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 43898-0123
Start Marketing Date : 2015-03-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 43898-0133
Start Marketing Date : 2015-03-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 48292-0012
Start Marketing Date : 2015-02-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 48292-0013
Start Marketing Date : 2015-02-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 48292-0014
Start Marketing Date : 2015-02-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Salbutamol Sulphate 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 Salbutamol Sulphate manufacturer or Salbutamol Sulphate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Salbutamol Sulphate manufacturer or Salbutamol Sulphate supplier.
PharmaCompass also assists you with knowing the Salbutamol Sulphate API Price utilized in the formulation of products. Salbutamol Sulphate API Price is not always fixed or binding as the Salbutamol Sulphate Price is obtained through a variety of data sources. The Salbutamol Sulphate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Albuterol Sulfate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Albuterol Sulfate, including repackagers and relabelers. The FDA regulates Albuterol Sulfate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Albuterol Sulfate 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 Albuterol Sulfate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Albuterol Sulfate supplier is an individual or a company that provides Albuterol Sulfate active pharmaceutical ingredient (API) or Albuterol Sulfate finished formulations upon request. The Albuterol Sulfate suppliers may include Albuterol Sulfate API manufacturers, exporters, distributors and traders.
click here to find a list of Albuterol Sulfate 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 Albuterol Sulfate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Albuterol Sulfate 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 Albuterol Sulfate 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 Albuterol Sulfate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Albuterol Sulfate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Albuterol Sulfate suppliers with NDC on PharmaCompass.
We have 15 companies offering Albuterol Sulfate
Get in contact with the supplier of your choice: