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rexall bismuth
rexall bismuth - 55910-469-65 - (Bismuth subsalicylate)
Drug Information of rexall bismuth
| Product NDC: | 55910-469 |
| Proprietary Name: | rexall bismuth |
| 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 rexall bismuth
| Product NDC: | 55910-469 |
| Labeler Name: | Dolgencorp Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part335 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120928 |
Package Information of rexall bismuth
| Package NDC: | 55910-469-65 |
| Package Description: | 5 BLISTER PACK in 1 CARTON (55910-469-65) > 6 TABLET, CHEWABLE in 1 BLISTER PACK |
NDC Information of rexall bismuth
| NDC Code | 55910-469-65 |
| Proprietary Name | rexall bismuth |
| Package Description | 5 BLISTER PACK in 1 CARTON (55910-469-65) > 6 TABLET, CHEWABLE in 1 BLISTER PACK |
| Product NDC | 55910-469 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Bismuth subsalicylate |
| Dosage Form Name | TABLET, CHEWABLE |
| Route Name | ORAL |
| Start Marketing Date | 20120928 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Dolgencorp Inc |
| Substance Name | BISMUTH SUBSALICYLATE |
| Strength Number | 262 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
