Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 017957

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NOVAMINE 11.4% (AMINO ACIDS)
11.4% (11.4GM/100ML)
Marketing Status: Discontinued

Active Ingredient: AMINO ACIDS
Proprietary Name: NOVAMINE 11.4%
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 11.4% (11.4GM/100ML)
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N017957
Product Number: 003
Approval Date: Aug 9, 1982
Applicant Holder Full Name: HOSPIRA INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

NOVAMINE 15% (AMINO ACIDS)
15% (75GM/500ML)
Marketing Status: Discontinued

Active Ingredient: AMINO ACIDS
Proprietary Name: NOVAMINE 15%
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 15% (75GM/500ML)
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N017957
Product Number: 004
Approval Date: Nov 28, 1986
Applicant Holder Full Name: HOSPIRA INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

NOVAMINE 8.5% (AMINO ACIDS)
8.5% (8.5GM/100ML)
Marketing Status: Discontinued

Active Ingredient: AMINO ACIDS
Proprietary Name: NOVAMINE 8.5%
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 8.5% (8.5GM/100ML)
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N017957
Product Number: 002
Approval Date: Aug 9, 1982
Applicant Holder Full Name: HOSPIRA INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

VEINAMINE 8% (AMINO ACIDS; MAGNESIUM CHLORIDE; POTASSIUM ACETATE; POTASSIUM CHLORIDE; SODIUM ACETATE)
8%;61MG/100ML;211MG/100ML;56MG/100ML;388MG/100ML
Marketing Status: Discontinued

Active Ingredient: AMINO ACIDS; MAGNESIUM CHLORIDE; POTASSIUM ACETATE; POTASSIUM CHLORIDE; SODIUM ACETATE
Proprietary Name: VEINAMINE 8%
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 8%;61MG/100ML;211MG/100ML;56MG/100ML;388MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N017957
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: HOSPIRA INC
Marketing Status:  Discontinued
Patent and Exclusivity Information