Product NDC: | 0121-4803 |
Proprietary Name: | Pink Bismuth |
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: | 0121-4803 |
Labeler Name: | Pharmaceutical Associates, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part335 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20090920 |
Package NDC: | 0121-4803-30 |
Package Description: | 4 TRAY in 1 CASE (0121-4803-30) > 10 CUP, UNIT-DOSE in 1 TRAY > 30 mL in 1 CUP, UNIT-DOSE |
NDC Code | 0121-4803-30 |
Proprietary Name | Pink Bismuth |
Package Description | 4 TRAY in 1 CASE (0121-4803-30) > 10 CUP, UNIT-DOSE in 1 TRAY > 30 mL in 1 CUP, UNIT-DOSE |
Product NDC | 0121-4803 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Bismuth Subsalicylate |
Dosage Form Name | SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 20090920 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Pharmaceutical Associates, Inc. |
Substance Name | BISMUTH SUBSALICYLATE |
Strength Number | 262 |
Strength Unit | mg/15mL |
Pharmaceutical Classes |