Product NDC: | 24202-002 |
Proprietary Name: | CALCID |
Non Proprietary Name: | Calcium carbonate |
Active Ingredient(s): | 500 mg/1 & nbsp; Calcium carbonate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, CHEWABLE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 24202-002 |
Labeler Name: | Pro-ventas S.A. de C.V. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part331 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20111230 |
Package NDC: | 24202-002-10 |
Package Description: | 100 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (24202-002-10) |
NDC Code | 24202-002-10 |
Proprietary Name | CALCID |
Package Description | 100 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (24202-002-10) |
Product NDC | 24202-002 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Calcium carbonate |
Dosage Form Name | TABLET, CHEWABLE |
Route Name | ORAL |
Start Marketing Date | 20111230 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Pro-ventas S.A. de C.V. |
Substance Name | CALCIUM CARBONATE |
Strength Number | 500 |
Strength Unit | mg/1 |
Pharmaceutical Classes |