Product NDC: | 0536-3504 |
Proprietary Name: | Almacone |
Non Proprietary Name: | Aluminum hydroxide, Magnesium hydroxide, Simethicone |
Active Ingredient(s): | 200; 20; 200 mg/1; mg/1; mg/1 & nbsp; Aluminum hydroxide, Magnesium hydroxide, Simethicone |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, CHEWABLE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0536-3504 |
Labeler Name: | Rugby Laboratories, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part332 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100823 |
Package NDC: | 0536-3504-01 |
Package Description: | 100 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (0536-3504-01) |
NDC Code | 0536-3504-01 |
Proprietary Name | Almacone |
Package Description | 100 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (0536-3504-01) |
Product NDC | 0536-3504 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Aluminum hydroxide, Magnesium hydroxide, Simethicone |
Dosage Form Name | TABLET, CHEWABLE |
Route Name | ORAL |
Start Marketing Date | 20100823 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Rugby Laboratories, Inc. |
Substance Name | ALUMINUM HYDROXIDE; DIMETHICONE; MAGNESIUM HYDROXIDE |
Strength Number | 200; 20; 200 |
Strength Unit | mg/1; mg/1; mg/1 |
Pharmaceutical Classes |