Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
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.
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
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
Neuland Laboratories- A dedicated 100% API provider.
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
A Ventolin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ventolin, including repackagers and relabelers. The FDA regulates Ventolin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ventolin 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 Ventolin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ventolin supplier is an individual or a company that provides Ventolin active pharmaceutical ingredient (API) or Ventolin finished formulations upon request. The Ventolin suppliers may include Ventolin API manufacturers, exporters, distributors and traders.
click here to find a list of Ventolin 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 Ventolin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Ventolin 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 Ventolin 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 Ventolin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Ventolin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Ventolin suppliers with NDC on PharmaCompass.
We have 15 companies offering Ventolin
Get in contact with the supplier of your choice:
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