Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

Home | Back to Search Results

Product Details for NDA 050565

Expand all

COACTIN (AMDINOCILLIN)
250MG/VIAL
Marketing Status: Discontinued

Active Ingredient: AMDINOCILLIN
Proprietary Name: COACTIN
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 250MG/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N050565
Product Number: 001
Approval Date: Dec 21, 1984
Applicant Holder Full Name: HOFFMANN LA ROCHE INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

COACTIN (AMDINOCILLIN)
500MG/VIAL
Marketing Status: Discontinued

Active Ingredient: AMDINOCILLIN
Proprietary Name: COACTIN
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 500MG/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N050565
Product Number: 002
Approval Date: Dec 21, 1984
Applicant Holder Full Name: HOFFMANN LA ROCHE INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

COACTIN (AMDINOCILLIN)
1GM/VIAL
Marketing Status: Discontinued

Active Ingredient: AMDINOCILLIN
Proprietary Name: COACTIN
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 1GM/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N050565
Product Number: 003
Approval Date: Dec 21, 1984
Applicant Holder Full Name: HOFFMANN LA ROCHE INC
Marketing Status:  Discontinued
Patent and Exclusivity Information