NebuPent (Fresenius Kabi USA, LLC)
Welcome to the PulseAid listing for the NebuPent drug offered from Fresenius Kabi USA, LLC. This Antiprotozoal [EPC] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
| LABELER NAME / MANUFACTURER: | Fresenius Kabi USA, LLC |
| NON-PROPRIETARY NAME: | PENTAMIDINE ISETHIONATE |
| SUBSTANCE NAME: | PENTAMIDINE ISETHIONATE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Antiprotozoal [EPC] |
| ROUTE: | RESPIRATORY (INHALATION) |
| DOSAGE FORM: | INHALANT |
| MARKETING CATEGORY NAME: | NDA |
| START MARKETING DATE: | 2011-02-15 |
| END MARKETING DATE: | 0000-00-00 |
NebuPent HUMAN PRESCRIPTION DRUG Details:
| Item Description | NebuPent from Fresenius Kabi USA, LLC |
| LABELER NAME: | Fresenius Kabi USA, LLC |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 300(mg/6mL) |
| START MARKETING DATE: | 2011-02-15 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 63323-877_9d14a7f6-afab-40d6-b3d2-4ebe8bed0605 |
| PRODUCT NDC: | 63323-877 |
| APPLICATION NUMBER: | NDA019887 |
Other PENTAMIDINE ISETHIONATE Pharmaceutical Manufacturers / Labelers:
