Product NDC: | 11822-0880 |
Proprietary Name: | antacid |
Non Proprietary Name: | Aluminum hydroxide, Magnesium carbonate |
Active Ingredient(s): | 160; 105 mg/1; mg/1 & nbsp; Aluminum hydroxide, Magnesium carbonate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, CHEWABLE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 11822-0880 |
Labeler Name: | Rite Aid Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part331 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 19970807 |
Package NDC: | 11822-0880-7 |
Package Description: | 100 TABLET, CHEWABLE in 1 BOTTLE (11822-0880-7) |
NDC Code | 11822-0880-7 |
Proprietary Name | antacid |
Package Description | 100 TABLET, CHEWABLE in 1 BOTTLE (11822-0880-7) |
Product NDC | 11822-0880 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Aluminum hydroxide, Magnesium carbonate |
Dosage Form Name | TABLET, CHEWABLE |
Route Name | ORAL |
Start Marketing Date | 19970807 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Rite Aid Corporation |
Substance Name | ALUMINUM HYDROXIDE; MAGNESIUM CARBONATE |
Strength Number | 160; 105 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes |