DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr. Reddy's Laboratories Limited
02 1Dr.Reddy's laboratories Limited
03 1Aurobindo Pharma Limited
04 1BioPhysics Pharma, Inc.
05 2Divi's Laboratories Limited
06 1Hetero Labs Limited
07 1LETCO MEDICAL, LLC
08 1Spectrum Laboratory Products, Inc.
09 2Zhejiang Charioteer Pharmaceutical Co., Ltd.
01 1NAPROXEN SODIUM
02 8Naproxen Sodium
03 1Naproxen Sodium Granule
04 1Naproxen sodium
01 2China
02 6India
03 3U.S.A
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
NDC Package Code : 30007-815
Start Marketing Date : 2012-02-06
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
NDC Package Code : 55111-004
Start Marketing Date : 1997-01-28
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65862-507
Start Marketing Date : 2024-01-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63310-2100
Start Marketing Date : 2012-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 63310-2070
Start Marketing Date : 2005-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62331-002
Start Marketing Date : 1999-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62331-030
Start Marketing Date : 2006-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 68554-0129
Start Marketing Date : 1994-11-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62991-2904
Start Marketing Date : 2010-11-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 49452-4817
Start Marketing Date : 1994-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
A Naproxen Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Naproxen Sodium, including repackagers and relabelers. The FDA regulates Naproxen Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Naproxen Sodium 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 Naproxen Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Naproxen Sodium supplier is an individual or a company that provides Naproxen Sodium active pharmaceutical ingredient (API) or Naproxen Sodium finished formulations upon request. The Naproxen Sodium suppliers may include Naproxen Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Naproxen Sodium 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 Naproxen Sodium as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Naproxen Sodium 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 Naproxen Sodium 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 Naproxen Sodium and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Naproxen Sodium NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Naproxen Sodium suppliers with NDC on PharmaCompass.
We have 8 companies offering Naproxen Sodium
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