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Theophylline in Dextrose - 0409-7668-23 - (THEOPHYLLINE)

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Drug Information of Theophylline in Dextrose

Product NDC: 0409-7668
Proprietary Name: Theophylline in Dextrose
Non Proprietary Name: THEOPHYLLINE
Active Ingredient(s): 200    mg/100mL & nbsp;   THEOPHYLLINE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Theophylline in Dextrose

Product NDC: 0409-7668
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019211
Marketing Category: NDA
Start Marketing Date: 19840102

Package Information of Theophylline in Dextrose

Package NDC: 0409-7668-23
Package Description: 24 BAG in 1 CASE (0409-7668-23) > 100 mL in 1 BAG

NDC Information of Theophylline in Dextrose

NDC Code 0409-7668-23
Proprietary Name Theophylline in Dextrose
Package Description 24 BAG in 1 CASE (0409-7668-23) > 100 mL in 1 BAG
Product NDC 0409-7668
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name THEOPHYLLINE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19840102
Marketing Category Name NDA
Labeler Name Hospira, Inc.
Substance Name THEOPHYLLINE
Strength Number 200
Strength Unit mg/100mL
Pharmaceutical Classes

Complete Information of Theophylline in Dextrose


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