Siegfried – A global CDMO delivering integrated pharmaceutical development and manufacturing solutions.
01 1Siegfried PharmaChemikalien Minden GmbH
02 1AX Pharmaceutical Corp.
03 1CTX Lifesciences Pvt. Ltd.
04 1DARMERICA, LLC
05 1LETCO MEDICAL, LLC
06 1Professional Compounding Centers of America dba PCCA
07 1Shodhana Laboratories Private Limited
08 1Spectrum Laboratory Products, Inc.
09 1Suresource Pharma LLC
01 2OXYMETAZOLINE HYDROCHLORIDE
02 2Oxymetazoline HCl
03 3Oxymetazoline Hydrochloride
04 1Oxymetazoline Hydrochloride Crystalline
05 1oxymetazoline hydrochloride
01 1Canada
02 2India
03 1Switzerland
04 3U.S.A
05 1United Kingdom
06 1Blank
Siegfried – A global CDMO delivering integrated pharmaceutical development and manufacturing solutions.
NDC Package Code : 65724-4503
Start Marketing Date : 2010-03-02
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 73377-324
Start Marketing Date : 2025-06-05
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 42419-005
Start Marketing Date : 2008-12-10
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 71052-482
Start Marketing Date : 2021-11-15
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62991-3201
Start Marketing Date : 2024-02-14
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-3205
Start Marketing Date : 2013-06-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 69056-005
Start Marketing Date : 2024-08-10
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-4954
Start Marketing Date : 2000-07-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 85694-002
Start Marketing Date : 2025-08-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
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A Benzedrex Nasal Spray 12 Hour manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Benzedrex Nasal Spray 12 Hour, including repackagers and relabelers. The FDA regulates Benzedrex Nasal Spray 12 Hour manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Benzedrex Nasal Spray 12 Hour API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Benzedrex Nasal Spray 12 Hour supplier is an individual or a company that provides Benzedrex Nasal Spray 12 Hour active pharmaceutical ingredient (API) or Benzedrex Nasal Spray 12 Hour finished formulations upon request. The Benzedrex Nasal Spray 12 Hour suppliers may include Benzedrex Nasal Spray 12 Hour API manufacturers, exporters, distributors and traders.
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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 Benzedrex Nasal Spray 12 Hour as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Benzedrex Nasal Spray 12 Hour 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 Benzedrex Nasal Spray 12 Hour 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 Benzedrex Nasal Spray 12 Hour and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Benzedrex Nasal Spray 12 Hour NDC to their finished compounded human drug products, they may choose to do so.
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We have 8 companies offering Benzedrex Nasal Spray 12 Hour
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