Product NDC: | 55154-4519 |
Proprietary Name: | Tums |
Non Proprietary Name: | Calcium Carbonate |
Active Ingredient(s): | 500 mg/1 & nbsp; Calcium Carbonate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55154-4519 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20110615 |
Package NDC: | 55154-4519-4 |
Package Description: | 150 POUCH in 1 CARTON (55154-4519-4) > 1 TABLET in 1 POUCH (55154-4519-6) |
NDC Code | 55154-4519-4 |
Proprietary Name | Tums |
Package Description | 150 POUCH in 1 CARTON (55154-4519-4) > 1 TABLET in 1 POUCH (55154-4519-6) |
Product NDC | 55154-4519 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Calcium Carbonate |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20110615 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Cardinal Health |
Substance Name | CALCIUM CARBONATE |
Strength Number | 500 |
Strength Unit | mg/1 |
Pharmaceutical Classes |