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