Product Details for NDA 018654
VERSED (MIDAZOLAM HYDROCHLORIDE)
EQ 1MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
EQ 5MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
EQ 1MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: MIDAZOLAM HYDROCHLORIDE
Proprietary Name: VERSED
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 1MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N018654
Product Number: 002
Approval Date: May 26, 1987
Applicant Holder Full Name: HLR TECHNOLOGY
Marketing Status: Discontinued
Patent and Exclusivity Information
VERSED (MIDAZOLAM HYDROCHLORIDE)
Proprietary Name: VERSED
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 1MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N018654
Product Number: 002
Approval Date: May 26, 1987
Applicant Holder Full Name: HLR TECHNOLOGY
Marketing Status: Discontinued
Patent and Exclusivity Information
EQ 5MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: MIDAZOLAM HYDROCHLORIDE
Proprietary Name: VERSED
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 5MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N018654
Product Number: 001
Approval Date: Dec 20, 1985
Applicant Holder Full Name: HLR TECHNOLOGY
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: VERSED
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 5MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N018654
Product Number: 001
Approval Date: Dec 20, 1985
Applicant Holder Full Name: HLR TECHNOLOGY
Marketing Status: Discontinued
Patent and Exclusivity Information