Product NDC: | 0603-0213 |
Proprietary Name: | Magnesium Oxide |
Non Proprietary Name: | Magnesium Oxide |
Active Ingredient(s): | 253 mg/1 & nbsp; Magnesium Oxide |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0603-0213 |
Labeler Name: | Qualitest Pharmaceuticals |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part331 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20031006 |
Package NDC: | 0603-0213-21 |
Package Description: | 100 TABLET in 1 BOTTLE (0603-0213-21) |
NDC Code | 0603-0213-21 |
Proprietary Name | Magnesium Oxide |
Package Description | 100 TABLET in 1 BOTTLE (0603-0213-21) |
Product NDC | 0603-0213 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Magnesium Oxide |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20031006 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Qualitest Pharmaceuticals |
Substance Name | MAGNESIUM OXIDE |
Strength Number | 253 |
Strength Unit | mg/1 |
Pharmaceutical Classes |