55259-0001 NDC - 7030 CALCIUM GOLD (CALCIUM)

Drug Information

Product NDC: 55259-0001

Proprietary Name: 7030 Calcium Gold

Non Proprietary Name: CALCIUM

Active Ingredient(s):
  • .99 1/1 CALCIUM


Administration Route(s): ORAL

Dosage Form(s): CAPSULE

Pharmacy Class(es):
  • Calcium [CS];
  • Calcium [EPC];
  • Phosphate Binder [EPC];
  • Phosphate Chelating Activity [MoA]

Labeler Information

Labeler Name: Apexel Co., Ltd
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date:3/18/2021

Package Information

No. Package Code Package Description Billing Unit
155259-0001-1120 CAPSULE in 1 PACKAGE (55259-0001-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC55259-0001The 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 NAMEHUMAN OTC DRUGIndicates 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 NAME7030 Calcium GoldThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMECALCIUMThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMECAPSULEThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE3/18/2021This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED DRUG OTHERProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMEApexel Co., LtdName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMECALCIUMAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH.99 
ACTIVE INGRED UNIT1/1 
PHARM CLASSESCalcium [CS], Calcium [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA] 

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This page was last updated on: 2/1/2023