Product NDC: | 59779-015 |
Proprietary Name: | Antacid Supreme |
Non Proprietary Name: | ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE |
Active Ingredient(s): | 400; 135 mg/5mL; mg/5mL & nbsp; ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE |
Administration Route(s): | ORAL |
Dosage Form(s): | SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59779-015 |
Labeler Name: | CVS |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part331 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20090107 |
Package NDC: | 59779-015-12 |
Package Description: | 355 mL in 1 BOTTLE, PLASTIC (59779-015-12) |
NDC Code | 59779-015-12 |
Proprietary Name | Antacid Supreme |
Package Description | 355 mL in 1 BOTTLE, PLASTIC (59779-015-12) |
Product NDC | 59779-015 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE |
Dosage Form Name | SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 20090107 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | CVS |
Substance Name | ALUMINUM HYDROXIDE; MAGNESIUM HYDROXIDE |
Strength Number | 400; 135 |
Strength Unit | mg/5mL; mg/5mL |
Pharmaceutical Classes |