Product NDC: | 46084-071 |
Proprietary Name: | APCAL |
Non Proprietary Name: | Calcium Carbonate and Vitamin D3 |
Active Ingredient(s): | 1250; 250 mg/1; [iU]/1 & nbsp; Calcium Carbonate and Vitamin D3 |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 46084-071 |
Labeler Name: | A P J Laboratories limited |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part331 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20130301 |
Package NDC: | 46084-071-14 |
Package Description: | 120 TABLET in 1 BLISTER PACK (46084-071-14) |
NDC Code | 46084-071-14 |
Proprietary Name | APCAL |
Package Description | 120 TABLET in 1 BLISTER PACK (46084-071-14) |
Product NDC | 46084-071 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Calcium Carbonate and Vitamin D3 |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20130301 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | A P J Laboratories limited |
Substance Name | CALCIUM CARBONATE; CHOLECALCIFEROL |
Strength Number | 1250; 250 |
Strength Unit | mg/1; [iU]/1 |
Pharmaceutical Classes |