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01 1Ailex Pharma
02 1B. Braun Medical
03 1Bausch & Lomb Incorporated
04 1Bayer AG
05 1Estilad
06 2Maia Pharmaceuticals
07 1Myungmoon Pharm. Co., LTD.
08 2Navinta
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01 1INJECTION;
02 1Lozenge
03 6SOLUTION;INTRAVENOUS
04 1SOLUTION;ORAL
05 1Solution
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01 1Cancelled
02 2DISCN
03 1Generic
04 5RX
05 1Blank
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01 1AMMONUL
02 1Dr. Andreu'S Pills
03 1Mezoca
04 5SODIUM PHENYLACETATE AND SODIUM BENZOATE
05 1UCEPHAN
06 1Blank
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01 1Canada
02 1South Korea
03 1Spain
04 7USA
Regulatory Info : RX
Registration Country : USA
SODIUM BENZOATE; SODIUM PHENYLACETATE
Brand Name : SODIUM PHENYLACETATE AND SODIUM BENZOATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : 10%;10% (5GM/50ML;5GM/50ML)
Packaging :
Approval Date : 2016-02-24
Application Number : 207096
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
SODIUM BENZOATE; SODIUM PHENYLACETATE
Brand Name : UCEPHAN
Dosage Form : SOLUTION;ORAL
Dosage Strength : 100MG/ML;100MG/ML
Packaging :
Approval Date : 1987-12-23
Application Number : 19530
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
SODIUM BENZOATE; SODIUM PHENYLACETATE
Brand Name : AMMONUL
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : 10%;10% (5GM/50ML;5GM/50ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 2005-02-17
Application Number : 20645
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : Cancelled
Registration Country : Spain
Sodium Benzoate; Dextromethorphan Hydrobromide
Brand Name : Dr. Andreu'S Pills
Dosage Form : Lozenge
Dosage Strength : 2MG; 15 MG
Packaging :
Approval Date : 1989-06-01
Application Number : 57875
Regulatory Info : Cancelled
Registration Country : Spain
Regulatory Info :
Registration Country : Canada
Sodium DNA; Sodium Hyaluronate; Sodium Chloride; GLYCERIN; GLUCONOLACTONE; Sodium Benzoate; Calcium Gluconate
Brand Name :
Dosage Form : Solution
Dosage Strength :
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Canada
Regulatory Info : RX
Registration Country : USA
SODIUM BENZOATE; SODIUM PHENYLACETATE
Brand Name : SODIUM PHENYLACETATE AND SODIUM BENZOATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : 10%;10% (5GM/50ML;5GM/50ML)
Packaging :
Approval Date : 2017-05-08
Application Number : 208521
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
SODIUM BENZOATE; SODIUM PHENYLACETATE
Brand Name : SODIUM PHENYLACETATE AND SODIUM BENZOATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : 10%;10% (2GM/20ML;2GM/20ML)
Packaging :
Approval Date : 2021-06-10
Application Number : 215025
Regulatory Info : RX
Registration Country : USA
Regulatory Info : Generic
Registration Country : South Korea
Brand Name : Mezoca
Dosage Form : INJECTION;
Dosage Strength : 220MG/2ML;
Packaging :
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Korea
Regulatory Info : RX
Registration Country : USA
SODIUM BENZOATE; SODIUM PHENYLACETATE
Brand Name : SODIUM PHENYLACETATE AND SODIUM BENZOATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : 10%;10% (5GM/50ML;5GM/50ML)
Packaging :
Approval Date : 2016-08-04
Application Number : 205880
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
SODIUM BENZOATE; SODIUM PHENYLACETATE
Brand Name : SODIUM PHENYLACETATE AND SODIUM BENZOATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : 10%;10% (2GM/20ML; 2GM/20ML)
Packaging :
Approval Date : 2023-07-14
Application Number : 217526
Regulatory Info : RX
Registration Country : USA