Aminophylline is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by General Injectables & Vaccines, Inc.. The primary component is Aminophylline Dihydrate.
| Product ID | 52584-922_408e04dd-8b86-44f0-acd7-38b77571a302 |
| NDC | 52584-922 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Aminophylline |
| Generic Name | Aminophylline |
| Dosage Form | Injection, Solution |
| Route of Administration | INTRAVENOUS |
| Marketing Start Date | 2009-01-01 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA087242 |
| Labeler Name | General Injectables & Vaccines, Inc. |
| Substance Name | AMINOPHYLLINE DIHYDRATE |
| Active Ingredient Strength | 25 mg/mL |
| Pharm Classes | Methylxanthine [EPC],Xanthines [CS] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 2009-01-01 |
| Marketing End Date | 2023-09-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA087242 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2009-01-01 |
| Ingredient | Strength |
|---|---|
| AMINOPHYLLINE DIHYDRATE | 25 mg/mL |
| SPL SET ID: | b15e5520-0a87-4943-9bbb-ead066456273 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0404-9813 | Aminophylline | Aminophylline |
| 0404-9814 | Aminophylline | Aminophylline |
| 0409-5921 | Aminophylline | Aminophylline |
| 0409-5922 | Aminophylline | Aminophylline |
| 51662-1204 | AMINOPHYLLINE | AMINOPHYLLINE |
| 51662-1341 | AMINOPHYLLINE | AMINOPHYLLINE |
| 52584-921 | Aminophylline | Aminophylline |
| 52584-922 | Aminophylline | Aminophylline |
| 55154-2366 | Aminophylline | Aminophylline Dihydrate |
| 55154-6987 | Aminophylline | Aminophylline Dihydrate |
| 71872-7060 | Aminophylline | Aminophylline |
| 71872-7121 | Aminophylline | Aminophylline |