Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 050618

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AMIKIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER (AMIKACIN SULFATE)
EQ 5MG BASE/ML
Marketing Status: Discontinued

Active Ingredient: AMIKACIN SULFATE
Proprietary Name: AMIKIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 5MG BASE/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N050618
Product Number: 002
Approval Date: Nov 30, 1987
Applicant Holder Full Name: APOTHECON INC DIV BRISTOL MYERS SQUIBB
Marketing Status:  Discontinued
Patent and Exclusivity Information

AMIKIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER (AMIKACIN SULFATE)
EQ 10MG BASE/ML
Marketing Status: Discontinued

Active Ingredient: AMIKACIN SULFATE
Proprietary Name: AMIKIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 10MG BASE/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N050618
Product Number: 001
Approval Date: Nov 30, 1987
Applicant Holder Full Name: APOTHECON INC DIV BRISTOL MYERS SQUIBB
Marketing Status:  Discontinued
Patent and Exclusivity Information