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Magnesium Oxide
Magnesium Oxide - 0603-0209-22 - (Magnesium Oxide)
Drug Information of Magnesium Oxide
| Product NDC: | 0603-0209 |
| Proprietary Name: | Magnesium Oxide |
| Non Proprietary Name: | Magnesium Oxide |
| Active Ingredient(s): | 400 mg/1 & nbsp; Magnesium Oxide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Magnesium Oxide
| Product NDC: | 0603-0209 |
| Labeler Name: | Qualitest Pharmaceutical, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part331 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20031203 |
Package Information of Magnesium Oxide
| Package NDC: | 0603-0209-22 |
| Package Description: | 120 TABLET in 1 BOTTLE (0603-0209-22) |
NDC Information of Magnesium Oxide
| NDC Code | 0603-0209-22 |
| Proprietary Name | Magnesium Oxide |
| Package Description | 120 TABLET in 1 BOTTLE (0603-0209-22) |
| Product NDC | 0603-0209 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Magnesium Oxide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20031203 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Qualitest Pharmaceutical, Inc. |
| Substance Name | MAGNESIUM OXIDE |
| Strength Number | 400 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
