Product NDC: | 63739-291 |
Proprietary Name: | Oyster Shell Calcium with Vitamin D |
Non Proprietary Name: | Oyster Shell Calcium with Vitamin D |
Active Ingredient(s): | 500; 200 mg/1; [iU]/1 & nbsp; Oyster Shell Calcium with Vitamin D |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63739-291 |
Labeler Name: | McKesson Packaging Services Business Unit of McKesson Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20051115 |
Package NDC: | 63739-291-01 |
Package Description: | 25 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-291-01) > 30 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Code | 63739-291-01 |
Proprietary Name | Oyster Shell Calcium with Vitamin D |
Package Description | 25 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-291-01) > 30 TABLET, FILM COATED in 1 BLISTER PACK |
Product NDC | 63739-291 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Oyster Shell Calcium with Vitamin D |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20051115 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | McKesson Packaging Services Business Unit of McKesson Corporation |
Substance Name | CALCIUM; CHOLECALCIFEROL |
Strength Number | 500; 200 |
Strength Unit | mg/1; [iU]/1 |
Pharmaceutical Classes |