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Magnesium Citrate
Magnesium Citrate - 49348-504-49 - (Magnesium citrate)
Drug Information of Magnesium Citrate
| Product NDC: | 49348-504 |
| Proprietary Name: | Magnesium Citrate |
| Non Proprietary Name: | Magnesium citrate |
| Active Ingredient(s): | 1.745 g/29.6mL & nbsp; Magnesium citrate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Magnesium Citrate
| Product NDC: | 49348-504 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20020301 |
Package Information of Magnesium Citrate
| Package NDC: | 49348-504-49 |
| Package Description: | .296 mL in 1 BOTTLE, GLASS (49348-504-49) |
NDC Information of Magnesium Citrate
| NDC Code | 49348-504-49 |
| Proprietary Name | Magnesium Citrate |
| Package Description | .296 mL in 1 BOTTLE, GLASS (49348-504-49) |
| Product NDC | 49348-504 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Magnesium citrate |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20020301 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | McKesson |
| Substance Name | MAGNESIUM CITRATE |
| Strength Number | 1.745 |
| Strength Unit | g/29.6mL |
| Pharmaceutical Classes |
