Product NDC: | 49580-0115 |
Proprietary Name: | Antacid Supreme Cherry |
Non Proprietary Name: | Mylanta Supreme Cherry |
Active Ingredient(s): | 400; 135 mg/5mL; mg/5mL & nbsp; Mylanta Supreme Cherry |
Administration Route(s): | ORAL |
Dosage Form(s): | SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49580-0115 |
Labeler Name: | Aaron Industries, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part331 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20090324 |
Package NDC: | 49580-0115-2 |
Package Description: | 355 mL in 1 BOTTLE, PLASTIC (49580-0115-2) |
NDC Code | 49580-0115-2 |
Proprietary Name | Antacid Supreme Cherry |
Package Description | 355 mL in 1 BOTTLE, PLASTIC (49580-0115-2) |
Product NDC | 49580-0115 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Mylanta Supreme Cherry |
Dosage Form Name | SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 20090324 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Aaron Industries, Inc. |
Substance Name | ALUMINUM HYDROXIDE; MAGNESIUM HYDROXIDE |
Strength Number | 400; 135 |
Strength Unit | mg/5mL; mg/5mL |
Pharmaceutical Classes |