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Active Ingredient: KETAMINE HYDROCHLORIDE
Proprietary Name: KETAMINE HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 10MG BASE/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: Application Number: A215808
Product Number: 001
Approval Date: Jan 13, 2023
Applicant Holder Full Name: FRESENIUS KABI USA LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information
Active Ingredient: KETAMINE HYDROCHLORIDE
Proprietary Name: KETAMINE HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 50MG BASE/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: Application Number: A215808
Product Number: 002
Approval Date: Jan 13, 2023
Applicant Holder Full Name: FRESENIUS KABI USA LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information
