Home
>
National Drug Code (NDC)
>
Pepto-Bismol
Pepto-Bismol - 37000-476-01 - (Bismuth subsalicylate)
Drug Information of Pepto-Bismol
| Product NDC: | 37000-476 |
| Proprietary Name: | Pepto-Bismol |
| Non Proprietary Name: | Bismuth subsalicylate |
| Active Ingredient(s): | 262 mg/1 & nbsp; Bismuth subsalicylate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pepto-Bismol
| Product NDC: | 37000-476 |
| Labeler Name: | Procter & Gamble Manufacturing Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part335 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20040630 |
Package Information of Pepto-Bismol
| Package NDC: | 37000-476-01 |
| Package Description: | 1 BLISTER PACK in 1 POUCH (37000-476-01) > 2 TABLET in 1 BLISTER PACK |
NDC Information of Pepto-Bismol
| NDC Code | 37000-476-01 |
| Proprietary Name | Pepto-Bismol |
| Package Description | 1 BLISTER PACK in 1 POUCH (37000-476-01) > 2 TABLET in 1 BLISTER PACK |
| Product NDC | 37000-476 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Bismuth subsalicylate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20040630 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Procter & Gamble Manufacturing Company |
| Substance Name | BISMUTH SUBSALICYLATE |
| Strength Number | 262 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
