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Approved Drug Products containing 215808 listed in the FDA Orange Book. Original Data : FDA Website

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01 2FRESENIUS KABI USA

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01

Brand Name : KETAMINE HYDROCHLORI...

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Brand Name : KETAMINE HYDROCHLORI...

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Fresenius Kabi USA

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : KETAMINE HYDROCHLORIDE

Dosage Strength : EQ 50MG BASE/ML

Approval Date : 2023-01-13

Application Number : 215808

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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02

Brand Name : KETAMINE HYDROCHLORI...

Luxepack
Not Confirmed
arrow

Brand Name : KETAMINE HYDROCHLORI...

Luxepack
Not Confirmed
arrow

Fresenius Kabi USA

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : KETAMINE HYDROCHLORIDE

Dosage Strength : EQ 10MG BASE/ML

Approval Date : 2023-01-13

Application Number : 215808

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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