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Estomarol
Estomarol - 57465-100-00 - (ALUMINUM HYDROXIDE, BISMUTH SUBCARBONATE, CALCIUM CARBONATE, MAGNESIUM CARBONATE, SODIUM BICARBONATE)
Drug Information of Estomarol
| Product NDC: | 57465-100 |
| Proprietary Name: | Estomarol |
| Non Proprietary Name: | ALUMINUM HYDROXIDE, BISMUTH SUBCARBONATE, CALCIUM CARBONATE, MAGNESIUM CARBONATE, SODIUM BICARBONATE |
| Active Ingredient(s): | .18; .21; .25; .59; 2.27 g/3.5g; g/3.5g; g/3.5g; g/3.5g; g/3.5g & nbsp; ALUMINUM HYDROXIDE, BISMUTH SUBCARBONATE, CALCIUM CARBONATE, MAGNESIUM CARBONATE, SODIUM BICARBONATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Estomarol
| Product NDC: | 57465-100 |
| Labeler Name: | Laboratorios Imperiales, S.A. de C.V. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part331 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110511 |
Package Information of Estomarol
| Package NDC: | 57465-100-00 |
| Package Description: | 15 PACKET in 1 BOX (57465-100-00) > 3.5 g in 1 PACKET |
NDC Information of Estomarol
| NDC Code | 57465-100-00 |
| Proprietary Name | Estomarol |
| Package Description | 15 PACKET in 1 BOX (57465-100-00) > 3.5 g in 1 PACKET |
| Product NDC | 57465-100 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ALUMINUM HYDROXIDE, BISMUTH SUBCARBONATE, CALCIUM CARBONATE, MAGNESIUM CARBONATE, SODIUM BICARBONATE |
| Dosage Form Name | POWDER |
| Route Name | ORAL |
| Start Marketing Date | 20110511 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Laboratorios Imperiales, S.A. de C.V. |
| Substance Name | ALUMINUM HYDROXIDE; BISMUTH SUBCARBONATE; CALCIUM CARBONATE; MAGNESIUM CARBONATE; SODIUM BICARBONATE |
| Strength Number | .18; .21; .25; .59; 2.27 |
| Strength Unit | g/3.5g; g/3.5g; g/3.5g; g/3.5g; g/3.5g |
| Pharmaceutical Classes |
