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 |