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APCAL
APCAL - 46084-071-16 - (Calcium Carbonate and Vitamin D3)
Drug Information of APCAL
| 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) |
Labeler Information of APCAL
| 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 Information of APCAL
| Package NDC: | 46084-071-16 |
| Package Description: | 500 TABLET in 1 BLISTER PACK (46084-071-16) |
NDC Information of APCAL
| NDC Code | 46084-071-16 |
| Proprietary Name | APCAL |
| Package Description | 500 TABLET in 1 BLISTER PACK (46084-071-16) |
| 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 |
