Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 018924

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AMINOPHYLLINE IN SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER (AMINOPHYLLINE)
100MG/100ML
Marketing Status: Discontinued

Active Ingredient: AMINOPHYLLINE
Proprietary Name: AMINOPHYLLINE IN SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 100MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018924
Product Number: 001
Approval Date: Dec 12, 1984
Applicant Holder Full Name: HOSPIRA INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

AMINOPHYLLINE IN SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER (AMINOPHYLLINE)
200MG/100ML
Marketing Status: Discontinued

Active Ingredient: AMINOPHYLLINE
Proprietary Name: AMINOPHYLLINE IN SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 200MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018924
Product Number: 002
Approval Date: Dec 12, 1984
Applicant Holder Full Name: HOSPIRA INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

AMINOPHYLLINE IN SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER (AMINOPHYLLINE)
400MG/100ML
Marketing Status: Discontinued

Active Ingredient: AMINOPHYLLINE
Proprietary Name: AMINOPHYLLINE IN SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 400MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018924
Product Number: 003
Approval Date: Dec 12, 1984
Applicant Holder Full Name: HOSPIRA INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

AMINOPHYLLINE IN SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER (AMINOPHYLLINE)
500MG/100ML
Marketing Status: Discontinued

Active Ingredient: AMINOPHYLLINE
Proprietary Name: AMINOPHYLLINE IN SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 500MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018924
Product Number: 004
Approval Date: Dec 12, 1984
Applicant Holder Full Name: HOSPIRA INC
Marketing Status:  Discontinued
Patent and Exclusivity Information