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Pepto-Bismol
Pepto-Bismol - 37000-403-01 - (Bismuth Subsalicylate)
Drug Information of Pepto-Bismol
| Product NDC: | 37000-403 |
| Proprietary Name: | Pepto-Bismol |
| Non Proprietary Name: | Bismuth Subsalicylate |
| Active Ingredient(s): | & nbsp; Bismuth Subsalicylate |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pepto-Bismol
| Product NDC: | 37000-403 |
| Labeler Name: | Procter & Gamble Manufacturing Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part335 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120305 |
Package Information of Pepto-Bismol
| Package NDC: | 37000-403-01 |
| Package Description: | 1 KIT in 1 PACKAGE (37000-403-01) * 354 mL in 1 BOTTLE, PLASTIC (37000-032-03) * 1 BOTTLE, PLASTIC in 1 CARTON (37000-691-30) > 30 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC |
NDC Information of Pepto-Bismol
| NDC Code | 37000-403-01 |
| Proprietary Name | Pepto-Bismol |
| Package Description | 1 KIT in 1 PACKAGE (37000-403-01) * 354 mL in 1 BOTTLE, PLASTIC (37000-032-03) * 1 BOTTLE, PLASTIC in 1 CARTON (37000-691-30) > 30 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC |
| Product NDC | 37000-403 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Bismuth Subsalicylate |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20120305 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Procter & Gamble Manufacturing Company |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
