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Calcium Gluconate
Calcium Gluconate - 0517-3900-25 - (Calcium Gluconate)
Drug Information of Calcium Gluconate
| Product NDC: | 0517-3900 |
| Proprietary Name: | Calcium Gluconate |
| Non Proprietary Name: | Calcium Gluconate |
| Active Ingredient(s): | 98 mg/mL & nbsp; Calcium Gluconate |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Calcium Gluconate
| Product NDC: | 0517-3900 |
| Labeler Name: | American Regent, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19921201 |
Package Information of Calcium Gluconate
| Package NDC: | 0517-3900-25 |
| Package Description: | 25 VIAL, PHARMACY BULK PACKAGE in 1 TRAY (0517-3900-25) > 100 mL in 1 VIAL, PHARMACY BULK PACKAGE |
NDC Information of Calcium Gluconate
| NDC Code | 0517-3900-25 |
| Proprietary Name | Calcium Gluconate |
| Package Description | 25 VIAL, PHARMACY BULK PACKAGE in 1 TRAY (0517-3900-25) > 100 mL in 1 VIAL, PHARMACY BULK PACKAGE |
| Product NDC | 0517-3900 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Calcium Gluconate |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19921201 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | American Regent, Inc. |
| Substance Name | CALCIUM GLUCONATE MONOHYDRATE |
| Strength Number | 98 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Calcium [Chemical/Ingredient],Calcium [EPC],Phosphate Binder [EPC],Phosphate Chelating Activity [MoA] |
