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Sodium Phosphates
Sodium Phosphates - 0409-7391-72 - (SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE and SODIUM PHOSPHATE, DIBASIC ANHYDROUS)
Drug Information of Sodium Phosphates
| Product NDC: | 0409-7391 |
| Proprietary Name: | Sodium Phosphates |
| Non Proprietary Name: | SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE and SODIUM PHOSPHATE, DIBASIC ANHYDROUS |
| Active Ingredient(s): | 142; 276 mg/mL; mg/mL & nbsp; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE and SODIUM PHOSPHATE, DIBASIC ANHYDROUS |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sodium Phosphates
| Product NDC: | 0409-7391 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018892 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110831 |
Package Information of Sodium Phosphates
| Package NDC: | 0409-7391-72 |
| Package Description: | 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-7391-72) > 15 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Sodium Phosphates
| NDC Code | 0409-7391-72 |
| Proprietary Name | Sodium Phosphates |
| Package Description | 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-7391-72) > 15 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 0409-7391 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE and SODIUM PHOSPHATE, DIBASIC ANHYDROUS |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20110831 |
| Marketing Category Name | NDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | SODIUM PHOSPHATE, DIBASIC ANHYDROUS; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE |
| Strength Number | 142; 276 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |
