Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
01 1COHANCE LIFESCIENCES LIMITED
02 1VIRUPAKSHA ORGANICS LIMITED
03 1FDC Limited
04 1Fagron Inc
05 1LETCO MEDICAL, LLC
06 1Medisca Inc.
07 1Pharmaron Manufacturing Services (UK) Ltd
08 1Professional Compounding Centers of America
09 1Professional Compounding Centers of America dba PCCA
10 1SUN PHARMACEUTICAL INDUSTRIES, INC.
11 1Spectrum Chemicals and Laboratory Products
12 1Vasudha Pharma Chem Limited
13 1Village Pharma LLC
14 1W. R. Grace & C0.-Conn.
01 3FLURBIPROFEN
02 10Flurbiprofen
03 1flurbiprofen
01 5India
02 1Latvia
03 1Netherlands
04 5U.S.A
05 2United Kingdom
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
NDC Package Code : 17511-123
Start Marketing Date : 2020-01-17
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
With Virupaksha, you get a quality product with on-time delivery.
NDC Package Code : 51686-0004
Start Marketing Date : 2007-10-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51552-0818
Start Marketing Date : 2004-09-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 55545-0405
Start Marketing Date : 1991-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 22568-1093
Start Marketing Date : 2006-06-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-2739
Start Marketing Date : 2014-05-26
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-0008
Start Marketing Date : 2012-05-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-0219
Start Marketing Date : 2021-11-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 61891-001
Start Marketing Date : 2017-03-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-3178
Start Marketing Date : 1997-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Flurbiprofen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Flurbiprofen, including repackagers and relabelers. The FDA regulates Flurbiprofen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Flurbiprofen 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 Flurbiprofen manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Flurbiprofen supplier is an individual or a company that provides Flurbiprofen active pharmaceutical ingredient (API) or Flurbiprofen finished formulations upon request. The Flurbiprofen suppliers may include Flurbiprofen API manufacturers, exporters, distributors and traders.
click here to find a list of Flurbiprofen 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 Flurbiprofen as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Flurbiprofen 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 Flurbiprofen 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 Flurbiprofen and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Flurbiprofen NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Flurbiprofen suppliers with NDC on PharmaCompass.
We have 13 companies offering Flurbiprofen
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