Product NDC: | 76457-001 |
Proprietary Name: | Aluminum hydroxide and Magnesium carbonate |
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: | 76457-001 |
Labeler Name: | Simpex Pharma Pvt. Ltd |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part331 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20121115 |
Package NDC: | 76457-001-00 |
Package Description: | 1 BOTTLE in 1 CARTON (76457-001-00) > 100 TABLET, CHEWABLE in 1 BOTTLE |
NDC Code | 76457-001-00 |
Proprietary Name | Aluminum hydroxide and Magnesium carbonate |
Package Description | 1 BOTTLE in 1 CARTON (76457-001-00) > 100 TABLET, CHEWABLE in 1 BOTTLE |
Product NDC | 76457-001 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ALUMINUM HYDROXIDE, MAGNESIUM CARBONATE |
Dosage Form Name | TABLET, CHEWABLE |
Route Name | ORAL |
Start Marketing Date | 20121115 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Simpex Pharma Pvt. Ltd |
Substance Name | ALUMINUM HYDROXIDE; MAGNESIUM CARBONATE |
Strength Number | 160; 105 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes |