Product NDC: | 56062-595 |
Proprietary Name: | maximum strength |
Non Proprietary Name: | Calcium Carbonate |
Active Ingredient(s): | 1000 mg/1 & nbsp; Calcium Carbonate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, CHEWABLE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 56062-595 |
Labeler Name: | Publix Super Markets Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part331 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20020429 |
Package NDC: | 56062-595-23 |
Package Description: | 72 TABLET, CHEWABLE in 1 BOTTLE (56062-595-23) |
NDC Code | 56062-595-23 |
Proprietary Name | maximum strength |
Package Description | 72 TABLET, CHEWABLE in 1 BOTTLE (56062-595-23) |
Product NDC | 56062-595 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Calcium Carbonate |
Dosage Form Name | TABLET, CHEWABLE |
Route Name | ORAL |
Start Marketing Date | 20020429 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Publix Super Markets Inc |
Substance Name | CALCIUM CARBONATE |
Strength Number | 1000 |
Strength Unit | mg/1 |
Pharmaceutical Classes |