Product Details for NDA 020098
MIVACRON IN DEXTROSE 5% IN PLASTIC CONTAINER (MIVACURIUM CHLORIDE)
EQ 0.5MG BASE/ML
Marketing Status: Discontinued
EQ 50MG BASE/100ML
Marketing Status: Discontinued
EQ 2MG BASE/ML (EQ 2MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
EQ 10MG BASE/5ML (EQ 2MG BASE/ML)
Marketing Status: Discontinued
EQ 20MG BASE/10ML (EQ 2MG BASE/ML)
Marketing Status: Discontinued
EQ 0.5MG BASE/ML
Marketing Status: Discontinued
Active Ingredient: MIVACURIUM CHLORIDE
Proprietary Name: MIVACRON IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 0.5MG BASE/ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N020098
Product Number: 002
Approval Date: Jan 22, 1992
Applicant Holder Full Name: ABBVIE INC
Marketing Status: Discontinued
Patent and Exclusivity Information
MIVACRON IN DEXTROSE 5% IN PLASTIC CONTAINER (MIVACURIUM CHLORIDE)
Proprietary Name: MIVACRON IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 0.5MG BASE/ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N020098
Product Number: 002
Approval Date: Jan 22, 1992
Applicant Holder Full Name: ABBVIE INC
Marketing Status: Discontinued
Patent and Exclusivity Information
EQ 50MG BASE/100ML
Marketing Status: Discontinued
Active Ingredient: MIVACURIUM CHLORIDE
Proprietary Name: MIVACRON IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 50MG BASE/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N020098
Product Number: 003
Approval Date: Jan 22, 1992
Applicant Holder Full Name: ABBVIE INC
Marketing Status: Discontinued
Patent and Exclusivity Information
MIVACRON (MIVACURIUM CHLORIDE)
Proprietary Name: MIVACRON IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 50MG BASE/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N020098
Product Number: 003
Approval Date: Jan 22, 1992
Applicant Holder Full Name: ABBVIE INC
Marketing Status: Discontinued
Patent and Exclusivity Information
EQ 2MG BASE/ML (EQ 2MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: MIVACURIUM CHLORIDE
Proprietary Name: MIVACRON
Dosage Form; Route of Administration: SOLUTION; INTRAVENOUS
Strength: EQ 2MG BASE/ML (EQ 2MG 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: N020098
Product Number: 001
Approval Date: Jan 22, 1992
Applicant Holder Full Name: ABBVIE INC
Marketing Status: Discontinued
Patent and Exclusivity Information
MIVACRON (MIVACURIUM CHLORIDE)
Proprietary Name: MIVACRON
Dosage Form; Route of Administration: SOLUTION; INTRAVENOUS
Strength: EQ 2MG BASE/ML (EQ 2MG 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: N020098
Product Number: 001
Approval Date: Jan 22, 1992
Applicant Holder Full Name: ABBVIE INC
Marketing Status: Discontinued
Patent and Exclusivity Information
EQ 10MG BASE/5ML (EQ 2MG BASE/ML)
Marketing Status: Discontinued
Active Ingredient: MIVACURIUM CHLORIDE
Proprietary Name: MIVACRON
Dosage Form; Route of Administration: SOLUTION; INTRAVENOUS
Strength: EQ 10MG BASE/5ML (EQ 2MG BASE/ML)
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N020098
Product Number: 004
Approval Date: Jan 22, 1992
Applicant Holder Full Name: ABBVIE INC
Marketing Status: Discontinued
Patent and Exclusivity Information
MIVACRON (MIVACURIUM CHLORIDE)
Proprietary Name: MIVACRON
Dosage Form; Route of Administration: SOLUTION; INTRAVENOUS
Strength: EQ 10MG BASE/5ML (EQ 2MG BASE/ML)
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N020098
Product Number: 004
Approval Date: Jan 22, 1992
Applicant Holder Full Name: ABBVIE INC
Marketing Status: Discontinued
Patent and Exclusivity Information
EQ 20MG BASE/10ML (EQ 2MG BASE/ML)
Marketing Status: Discontinued
Active Ingredient: MIVACURIUM CHLORIDE
Proprietary Name: MIVACRON
Dosage Form; Route of Administration: SOLUTION; INTRAVENOUS
Strength: EQ 20MG BASE/10ML (EQ 2MG BASE/ML)
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N020098
Product Number: 005
Approval Date: Jan 22, 1992
Applicant Holder Full Name: ABBVIE INC
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: MIVACRON
Dosage Form; Route of Administration: SOLUTION; INTRAVENOUS
Strength: EQ 20MG BASE/10ML (EQ 2MG BASE/ML)
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N020098
Product Number: 005
Approval Date: Jan 22, 1992
Applicant Holder Full Name: ABBVIE INC
Marketing Status: Discontinued
Patent and Exclusivity Information