Product NDC: | 72036-004 |
Proprietary Name: | Antacid Antigas |
Non Proprietary Name: | Mylanta |
Active Ingredient(s): | 200; 200; 200 mg/5mL; mg/5mL; mg/5mL & nbsp; Mylanta |
Administration Route(s): | ORAL |
Dosage Form(s): | SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 72036-004 |
Labeler Name: | Harris Teeter |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part331 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100122 |
Package NDC: | 72036-004-12 |
Package Description: | 355 mL in 1 BOTTLE, PLASTIC (72036-004-12) |
NDC Code | 72036-004-12 |
Proprietary Name | Antacid Antigas |
Package Description | 355 mL in 1 BOTTLE, PLASTIC (72036-004-12) |
Product NDC | 72036-004 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Mylanta |
Dosage Form Name | SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 20100122 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Harris Teeter |
Substance Name | ALUMINUM HYDROXIDE; DIMETHICONE; MAGNESIUM HYDROXIDE |
Strength Number | 200; 200; 200 |
Strength Unit | mg/5mL; mg/5mL; mg/5mL |
Pharmaceutical Classes |