01 1AX Pharmaceutical Corp
02 2Advanced Rx Pharmacy of Tennessee, LLC
03 1Amoli Organics (A Division of Umedica Laboratories Pvt.Ltd.)
04 4Asclemed USA, Inc.
05 1Cheng Fong Chemical Co., Ltd.
06 1DARMERICA, LLC
07 3Dipharma Francis Srl
08 1Fagron Inc
09 1Galenova Inc
10 1Henan Dongtai Pharm Co., Ltd.
11 1Henan Dongtai Pharm Co.,Ltd.
12 1Kalchem International inc
13 1LETCO MEDICAL, LLC
14 1MEDISCA Inc.
15 1Medisca Inc.
16 1Olon SpA
17 1Professional Compounding Centers of America
18 1Professional Compounding Centers of America dba PCCA
19 1Spectrum Laboratory Products, Inc.
20 1Syn-Tech Chem. & Pharm. Co., Ltd.
21 1Unique Chemicals
22 1Xenex Laboratories Inc
23 2YUNG ZIP CHEMICAL INDUSTRIAL .CO., LTD.
01 6DICLOFENAC SODIUM
02 22Diclofenac Sodium
03 2Diclofenac sodium
01 3Canada
02 3China
03 2India
04 4Italy
05 1Netherlands
06 3Taiwan
07 10U.S.A
08 2United Kingdom
09 2Blank
NDC Package Code : 46438-0640
Start Marketing Date : 2016-09-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46438-0046
Start Marketing Date : 1987-01-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46438-0629
Start Marketing Date : 1987-01-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50335-0030
Start Marketing Date : 2022-09-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50335-0060
Start Marketing Date : 2022-12-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 48589-0005
Start Marketing Date : 2009-11-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-2683
Start Marketing Date : 2014-06-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 38779-2705
Start Marketing Date : 2018-10-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0409
Start Marketing Date : 2017-03-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-2581
Start Marketing Date : 2000-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
A Diclofenac Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Diclofenac Sodium, including repackagers and relabelers. The FDA regulates Diclofenac Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Diclofenac 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 Diclofenac Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Diclofenac Sodium supplier is an individual or a company that provides Diclofenac Sodium active pharmaceutical ingredient (API) or Diclofenac Sodium finished formulations upon request. The Diclofenac Sodium suppliers may include Diclofenac Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Diclofenac 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 Diclofenac Sodium as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Diclofenac 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 Diclofenac 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 Diclofenac Sodium and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Diclofenac Sodium NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Diclofenac Sodium suppliers with NDC on PharmaCompass.
We have 19 companies offering Diclofenac Sodium
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
