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Bismatrol
Bismatrol - 17856-1313-3 - (Bismuth Subsalicylate)
Drug Information of Bismatrol
| Product NDC: | 17856-1313 |
| Proprietary Name: | Bismatrol |
| Non Proprietary Name: | Bismuth Subsalicylate |
| Active Ingredient(s): | 262 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: | 17856-1313 |
| Labeler Name: | Atlantic Biologicals Corps |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part335 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20080530 |
Package Information of Bismatrol
| Package NDC: | 17856-1313-3 |
| Package Description: | 30 mL in 1 CUP (17856-1313-3) |
NDC Information of Bismatrol
| NDC Code | 17856-1313-3 |
| Proprietary Name | Bismatrol |
| Package Description | 30 mL in 1 CUP (17856-1313-3) |
| Product NDC | 17856-1313 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Bismuth Subsalicylate |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20080530 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Atlantic Biologicals Corps |
| Substance Name | BISMUTH SUBSALICYLATE |
| Strength Number | 262 |
| Strength Unit | mg/15mL |
| Pharmaceutical Classes |
