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Bismatrol
Bismatrol - 0904-1315-46 - (Bismuth subsalicylate)
Drug Information of Bismatrol
| Product NDC: | 0904-1315 |
| Proprietary Name: | Bismatrol |
| Non Proprietary Name: | Bismuth subsalicylate |
| Active Ingredient(s): | 262 mg/1 & nbsp; Bismuth subsalicylate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, CHEWABLE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Bismatrol
| Product NDC: | 0904-1315 |
| Labeler Name: | Major Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part335 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20030103 |
Package Information of Bismatrol
| Package NDC: | 0904-1315-46 |
| Package Description: | 5 BLISTER PACK in 1 CARTON (0904-1315-46) > 6 TABLET, CHEWABLE in 1 BLISTER PACK |
NDC Information of Bismatrol
| NDC Code | 0904-1315-46 |
| Proprietary Name | Bismatrol |
| Package Description | 5 BLISTER PACK in 1 CARTON (0904-1315-46) > 6 TABLET, CHEWABLE in 1 BLISTER PACK |
| Product NDC | 0904-1315 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Bismuth subsalicylate |
| Dosage Form Name | TABLET, CHEWABLE |
| Route Name | ORAL |
| Start Marketing Date | 20030103 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Major Pharmaceuticals |
| Substance Name | BISMUTH SUBSALICYLATE |
| Strength Number | 262 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
