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Theophylline in Dextrose
Theophylline in Dextrose - 0338-0439-03 - (Theophylline Anhydrous)
Drug Information of Theophylline in Dextrose
| Product NDC: | 0338-0439 |
| Proprietary Name: | Theophylline in Dextrose |
| Non Proprietary Name: | Theophylline Anhydrous |
| Active Ingredient(s): | 80 mg/100mL & nbsp; Theophylline Anhydrous |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Theophylline in Dextrose
| Product NDC: | 0338-0439 |
| Labeler Name: | Baxter Healthcare Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018649 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19820726 |
Package Information of Theophylline in Dextrose
| Package NDC: | 0338-0439-03 |
| Package Description: | 18 BAG in 1 CARTON (0338-0439-03) > 500 mL in 1 BAG |
NDC Information of Theophylline in Dextrose
| NDC Code | 0338-0439-03 |
| Proprietary Name | Theophylline in Dextrose |
| Package Description | 18 BAG in 1 CARTON (0338-0439-03) > 500 mL in 1 BAG |
| Product NDC | 0338-0439 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Theophylline Anhydrous |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19820726 |
| Marketing Category Name | NDA |
| Labeler Name | Baxter Healthcare Corporation |
| Substance Name | THEOPHYLLINE ANHYDROUS |
| Strength Number | 80 |
| Strength Unit | mg/100mL |
| Pharmaceutical Classes |
