Product NDC: | 0264-9554 |
Proprietary Name: | Theophylline in Dextrose |
Non Proprietary Name: | Theophylline Anhydrous and Dextrose |
Active Ingredient(s): | 5; 80 g/100mL; mg/100mL & nbsp; Theophylline Anhydrous and Dextrose |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0264-9554 |
Labeler Name: | B. Braun Medical Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA019826 |
Marketing Category: | NDA |
Start Marketing Date: | 19920814 |
Package NDC: | 0264-9554-10 |
Package Description: | 24 CONTAINER in 1 CASE (0264-9554-10) > 500 mL in 1 CONTAINER |
NDC Code | 0264-9554-10 |
Proprietary Name | Theophylline in Dextrose |
Package Description | 24 CONTAINER in 1 CASE (0264-9554-10) > 500 mL in 1 CONTAINER |
Product NDC | 0264-9554 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Theophylline Anhydrous and Dextrose |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 19920814 |
Marketing Category Name | NDA |
Labeler Name | B. Braun Medical Inc. |
Substance Name | DEXTROSE MONOHYDRATE; THEOPHYLLINE ANHYDROUS |
Strength Number | 5; 80 |
Strength Unit | g/100mL; mg/100mL |
Pharmaceutical Classes | Methylxanthine [EPC],Xanthines [Chemical/Ingredient] |