Product NDC: | 41163-302 |
Proprietary Name: | Peptic Relief |
Non Proprietary Name: | Bismuth Subsalicylate |
Active Ingredient(s): | 262 mg/15mL & nbsp; Bismuth Subsalicylate |
Administration Route(s): | ORAL |
Dosage Form(s): | SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 41163-302 |
Labeler Name: | Equaline |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part335 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20090320 |
Package NDC: | 41163-302-40 |
Package Description: | 355 mL in 1 BOTTLE, PLASTIC (41163-302-40) |
NDC Code | 41163-302-40 |
Proprietary Name | Peptic Relief |
Package Description | 355 mL in 1 BOTTLE, PLASTIC (41163-302-40) |
Product NDC | 41163-302 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Bismuth Subsalicylate |
Dosage Form Name | SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 20090320 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Equaline |
Substance Name | BISMUTH SUBSALICYLATE |
Strength Number | 262 |
Strength Unit | mg/15mL |
Pharmaceutical Classes |