Sodium Phosphates (Hospira, Inc.)
Welcome to the PulseAid listing for the Sodium Phosphates drug offered from Hospira, Inc.. This 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: | Hospira, Inc. |
| NON-PROPRIETARY NAME: | SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE and SODIUM PHOSPHATE, DIBASIC, ANHYDROUS |
| SUBSTANCE NAME: | SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE; SODIUM PHOSPHATE, DIBASIC, ANHYDROUS |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | |
| ROUTE: | INTRAVENOUS |
| DOSAGE FORM: | INJECTION, SOLUTION |
| MARKETING CATEGORY NAME: | NDA |
| START MARKETING DATE: | 2005-06-02 |
| END MARKETING DATE: | 0000-00-00 |
Sodium Phosphates HUMAN PRESCRIPTION DRUG Details:
| Item Description | Sodium Phosphates from Hospira, Inc. |
| LABELER NAME: | Hospira, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 276; 142(mg/mL; mg/mL) |
| START MARKETING DATE: | 2005-06-02 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0409-7391_c8cbcd2d-9d3a-470e-8201-00c24e7b85c7 |
| PRODUCT NDC: | 0409-7391 |
| APPLICATION NUMBER: | NDA018892 |
Other SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE; SODIUM PHOSPHATE, DIBASIC, ANHYDROUS Pharmaceutical Manufacturers / Labelers:
