| Product NDC: | 52584-922 |
| Proprietary Name: | Aminophylline |
| Non Proprietary Name: | Aminophylline |
| Active Ingredient(s): | 25 mg/mL & nbsp; Aminophylline |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 52584-922 |
| Labeler Name: | General Injectables & Vaccines, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA087242 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090101 |
| Package NDC: | 52584-922-01 |
| Package Description: | 1 VIAL, SINGLE-DOSE in 1 BAG (52584-922-01) > 20 mL in 1 VIAL, SINGLE-DOSE |
| NDC Code | 52584-922-01 |
| Proprietary Name | Aminophylline |
| Package Description | 1 VIAL, SINGLE-DOSE in 1 BAG (52584-922-01) > 20 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 52584-922 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Aminophylline |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20090101 |
| Marketing Category Name | ANDA |
| Labeler Name | General Injectables & Vaccines, Inc. |
| Substance Name | AMINOPHYLLINE DIHYDRATE |
| Strength Number | 25 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |