Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 018649

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THEOPHYLLINE AND DEXTROSE 5% IN PLASTIC CONTAINER (THEOPHYLLINE)
4MG/ML
Marketing Status: Discontinued

Active Ingredient: THEOPHYLLINE
Proprietary Name: THEOPHYLLINE AND DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 4MG/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018649
Product Number: 007
Approval Date: Jul 26, 1982
Applicant Holder Full Name: BAXTER HEALTHCARE CORP
Marketing Status:  Discontinued
Patent and Exclusivity Information

THEOPHYLLINE AND DEXTROSE 5% IN PLASTIC CONTAINER (THEOPHYLLINE)
40MG/100ML
Marketing Status: Discontinued

Active Ingredient: THEOPHYLLINE
Proprietary Name: THEOPHYLLINE AND DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 40MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018649
Product Number: 001
Approval Date: Jul 26, 1982
Applicant Holder Full Name: BAXTER HEALTHCARE CORP
Marketing Status:  Discontinued
Patent and Exclusivity Information

THEOPHYLLINE AND DEXTROSE 5% IN PLASTIC CONTAINER (THEOPHYLLINE)
80MG/100ML
Marketing Status: Discontinued

Active Ingredient: THEOPHYLLINE
Proprietary Name: THEOPHYLLINE AND DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 80MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018649
Product Number: 002
Approval Date: Jul 26, 1982
Applicant Holder Full Name: BAXTER HEALTHCARE CORP
Marketing Status:  Discontinued
Patent and Exclusivity Information

THEOPHYLLINE AND DEXTROSE 5% IN PLASTIC CONTAINER (THEOPHYLLINE)
160MG/100ML
Marketing Status: Discontinued

Active Ingredient: THEOPHYLLINE
Proprietary Name: THEOPHYLLINE AND DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 160MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018649
Product Number: 003
Approval Date: Jul 26, 1982
Applicant Holder Full Name: BAXTER HEALTHCARE CORP
Marketing Status:  Discontinued
Patent and Exclusivity Information

THEOPHYLLINE AND DEXTROSE 5% IN PLASTIC CONTAINER (THEOPHYLLINE)
200MG/100ML
Marketing Status: Discontinued

Active Ingredient: THEOPHYLLINE
Proprietary Name: THEOPHYLLINE AND DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 200MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018649
Product Number: 004
Approval Date: Jul 26, 1982
Applicant Holder Full Name: BAXTER HEALTHCARE CORP
Marketing Status:  Discontinued
Patent and Exclusivity Information

THEOPHYLLINE AND DEXTROSE 5% IN PLASTIC CONTAINER (THEOPHYLLINE)
320MG/100ML
Marketing Status: Discontinued

Active Ingredient: THEOPHYLLINE
Proprietary Name: THEOPHYLLINE AND DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 320MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018649
Product Number: 006
Approval Date: Nov 13, 1985
Applicant Holder Full Name: BAXTER HEALTHCARE CORP
Marketing Status:  Discontinued
Patent and Exclusivity Information

THEOPHYLLINE AND DEXTROSE 5% IN PLASTIC CONTAINER (THEOPHYLLINE)
400MG/100ML
Marketing Status: Discontinued

Active Ingredient: THEOPHYLLINE
Proprietary Name: THEOPHYLLINE AND DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 400MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018649
Product Number: 005
Approval Date: Jul 26, 1982
Applicant Holder Full Name: BAXTER HEALTHCARE CORP
Marketing Status:  Discontinued
Patent and Exclusivity Information