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Bismatrol
Bismatrol - 0904-1314-09 - (Bismuth Subsalicylate)
Drug Information of Bismatrol
| Product NDC: | 0904-1314 |
| Proprietary Name: | Bismatrol |
| Non Proprietary Name: | Bismuth Subsalicylate |
| Active Ingredient(s): | 525 mg/15mL & nbsp; Bismuth Subsalicylate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Bismatrol
| Product NDC: | 0904-1314 |
| Labeler Name: | Major Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part335 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090105 |
Package Information of Bismatrol
| Package NDC: | 0904-1314-09 |
| Package Description: | 236 mL in 1 BOTTLE (0904-1314-09) |
NDC Information of Bismatrol
| NDC Code | 0904-1314-09 |
| Proprietary Name | Bismatrol |
| Package Description | 236 mL in 1 BOTTLE (0904-1314-09) |
| Product NDC | 0904-1314 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Bismuth Subsalicylate |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20090105 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Major Pharmaceuticals |
| Substance Name | BISMUTH SUBSALICYLATE |
| Strength Number | 525 |
| Strength Unit | mg/15mL |
| Pharmaceutical Classes |
