Product NDC: | 52567-001 |
Proprietary Name: | Brioschi Effervescent Antacid |
Non Proprietary Name: | sodium bicarbonate, tartaric acid |
Active Ingredient(s): | 1.8; 1.63 g/6g; g/6g & nbsp; sodium bicarbonate, tartaric acid |
Administration Route(s): | ORAL |
Dosage Form(s): | GRANULE, EFFERVESCENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52567-001 |
Labeler Name: | Brioschi Pharmaceuticals International, LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part331 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100920 |
Package NDC: | 52567-001-01 |
Package Description: | 240 g in 1 BOTTLE (52567-001-01) |
NDC Code | 52567-001-01 |
Proprietary Name | Brioschi Effervescent Antacid |
Package Description | 240 g in 1 BOTTLE (52567-001-01) |
Product NDC | 52567-001 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | sodium bicarbonate, tartaric acid |
Dosage Form Name | GRANULE, EFFERVESCENT |
Route Name | ORAL |
Start Marketing Date | 20100920 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Brioschi Pharmaceuticals International, LLC |
Substance Name | SODIUM BICARBONATE; TARTARIC ACID |
Strength Number | 1.8; 1.63 |
Strength Unit | g/6g; g/6g |
Pharmaceutical Classes |