Product NDC: | 0054-3117 |
Proprietary Name: | Calcium Carbonate |
Non Proprietary Name: | Calcium Carbonate |
Active Ingredient(s): | 1250 mg/5mL & nbsp; Calcium Carbonate |
Administration Route(s): | ORAL |
Dosage Form(s): | SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0054-3117 |
Labeler Name: | Roxane Laboratories, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part331 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20091124 |
Package NDC: | 0054-3117-63 |
Package Description: | 500 mL in 1 BOTTLE (0054-3117-63) |
NDC Code | 0054-3117-63 |
Proprietary Name | Calcium Carbonate |
Package Description | 500 mL in 1 BOTTLE (0054-3117-63) |
Product NDC | 0054-3117 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Calcium Carbonate |
Dosage Form Name | SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 20091124 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Roxane Laboratories, Inc. |
Substance Name | CALCIUM CARBONATE |
Strength Number | 1250 |
Strength Unit | mg/5mL |
Pharmaceutical Classes |