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Aminophylline
Aminophylline - 0409-5922-01 - (Aminophylline Dihydrate)
Drug Information of Aminophylline
| Product NDC: | 0409-5922 |
| Proprietary Name: | Aminophylline |
| Non Proprietary Name: | Aminophylline Dihydrate |
| Active Ingredient(s): | 25 mg/mL & nbsp; Aminophylline Dihydrate |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Aminophylline
| Product NDC: | 0409-5922 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA087242 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110211 |
Package Information of Aminophylline
| Package NDC: | 0409-5922-01 |
| Package Description: | 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-5922-01) > 20 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Aminophylline
| NDC Code | 0409-5922-01 |
| Proprietary Name | Aminophylline |
| Package Description | 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-5922-01) > 20 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 0409-5922 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Aminophylline Dihydrate |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20110211 |
| Marketing Category Name | ANDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | AMINOPHYLLINE DIHYDRATE |
| Strength Number | 25 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
