Home
>
National Drug Code (NDC)
>
BISMOL
BISMOL - 49789-080-01 - (BISMUTH SUBSALICYLATE)
Drug Information of BISMOL
| Product NDC: | 49789-080 |
| Proprietary Name: | BISMOL |
| Non Proprietary Name: | BISMUTH SUBSALICYLATE |
| Active Ingredient(s): | 262 mg/434mg & nbsp; BISMUTH SUBSALICYLATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BISMOL
| Product NDC: | 49789-080 |
| Labeler Name: | SAMSUNG PHARM IND. CO., LTD. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part335 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130201 |
Package Information of BISMOL
| Package NDC: | 49789-080-01 |
| Package Description: | 434 mg in 1 BLISTER PACK (49789-080-01) |
NDC Information of BISMOL
| NDC Code | 49789-080-01 |
| Proprietary Name | BISMOL |
| Package Description | 434 mg in 1 BLISTER PACK (49789-080-01) |
| Product NDC | 49789-080 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BISMUTH SUBSALICYLATE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130201 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | SAMSUNG PHARM IND. CO., LTD. |
| Substance Name | BISMUTH SUBSALICYLATE |
| Strength Number | 262 |
| Strength Unit | mg/434mg |
| Pharmaceutical Classes |
