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rexall bismuth
rexall bismuth - 55910-337-40 - (Bismuth subsalicylate)
Drug Information of rexall bismuth
| Product NDC: | 55910-337 |
| Proprietary Name: | rexall bismuth |
| 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 rexall bismuth
| Product NDC: | 55910-337 |
| Labeler Name: | Dolgencorp, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part335 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120906 |
Package Information of rexall bismuth
| Package NDC: | 55910-337-40 |
| Package Description: | 355 mL in 1 BOTTLE (55910-337-40) |
NDC Information of rexall bismuth
| NDC Code | 55910-337-40 |
| Proprietary Name | rexall bismuth |
| Package Description | 355 mL in 1 BOTTLE (55910-337-40) |
| Product NDC | 55910-337 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Bismuth subsalicylate |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20120906 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Dolgencorp, LLC |
| Substance Name | BISMUTH SUBSALICYLATE |
| Strength Number | 525 |
| Strength Unit | mg/15mL |
| Pharmaceutical Classes |
