| PRODUCT NDC | 55259-1112 | The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC. |
| PRODUCT TYPE NAME | HUMAN OTC DRUG | Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing. |
| PROPRIETARY NAME | 7030 Calcium Premium | The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes. |
| NON PROPRIETARY NAME | CALCIUM | The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product. |
| DOSAGE FORM NAME | CAPSULE | The translation of the dosage form Code submitted by the firm. |
| ROUTE NAME | ORAL | The translation of the route code submitted by the firm, indicating route of administration. |
| START MARKETING DATE | 3/18/2021 | This is the date that the labeler indicates was the start of its marketing of the drug product. |
| MARKETING CATEGORY NAME | UNAPPROVED DRUG OTHER | The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes. |
| LABELER NAME | Apexel Co., Ltd | This is the date that the labeler indicates was the start of its marketing of the drug product. |
| SUBSTANCE NAME | CALCIUM | Name of Company corresponding to the labeler code segment of the Product NDC. |
| ACTIVE NUMERATOR STRENGTH | .99 | |
| ACTIVE INGRED UNIT | mg/1 | |
| PHARM CLASSES | Calcium [CS], Calcium [EPC] | |