01 1AILEX PHARMS LLC
02 1B BRAUN
03 1BAUSCH
04 2MAIA PHARMS INC
05 2NAVINTA LLC
01 6SOLUTION;INTRAVENOUS
02 1SOLUTION;ORAL
01 2DISCN
02 5RX
01 1AMMONUL
02 5SODIUM PHENYLACETATE AND SODIUM BENZOATE
03 1UCEPHAN
01 5No
02 2Yes
RLD : No
TE Code : AP
SODIUM BENZOATE; SODIUM PHENYLACETATE
Brand Name : SODIUM PHENYLACETATE AND SODIUM BENZOATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : 10%;10% (5GM/50ML;5GM/50ML)
Approval Date : 2016-02-24
Application Number : 207096
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
RLD : No
TE Code :
SODIUM BENZOATE; SODIUM PHENYLACETATE
Brand Name : UCEPHAN
Dosage Form : SOLUTION;ORAL
Dosage Strength : 100MG/ML;100MG/ML
Approval Date : 1987-12-23
Application Number : 19530
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
SODIUM BENZOATE; SODIUM PHENYLACETATE
Brand Name : AMMONUL
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : 10%;10% (5GM/50ML;5GM/50ML)
Approval Date : 2005-02-17
Application Number : 20645
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code : AP
SODIUM BENZOATE; SODIUM PHENYLACETATE
Brand Name : SODIUM PHENYLACETATE AND SODIUM BENZOATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : 10%;10% (5GM/50ML;5GM/50ML)
Approval Date : 2017-05-08
Application Number : 208521
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
RLD : Yes
TE Code : AP
SODIUM BENZOATE; SODIUM PHENYLACETATE
Brand Name : SODIUM PHENYLACETATE AND SODIUM BENZOATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : 10%;10% (2GM/20ML;2GM/20ML)
Approval Date : 2021-06-10
Application Number : 215025
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AP
RLD : No
TE Code : AP
SODIUM BENZOATE; SODIUM PHENYLACETATE
Brand Name : SODIUM PHENYLACETATE AND SODIUM BENZOATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : 10%;10% (5GM/50ML;5GM/50ML)
Approval Date : 2016-08-04
Application Number : 205880
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
RLD : No
TE Code : AP
SODIUM BENZOATE; SODIUM PHENYLACETATE
Brand Name : SODIUM PHENYLACETATE AND SODIUM BENZOATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : 10%;10% (2GM/20ML; 2GM/20ML)
Approval Date : 2023-07-14
Application Number : 217526
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
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