Home NDC 55259-1112 7030 Calcium Premium
Product NDC 55259-1112
11-digit product format 552591112
Labeler code 55259
Product ID 55259-1112_0fa8135f-89c9-41a2-e063-6294a90a403d
Type HUMAN OTC DRUG
Nonproprietary name CALCIUM
Dosage form CAPSULE
Route ORAL
Labeler Apexel Co., Ltd
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2021-03-18
Substance CALCIUM
Active strength .99 mg/1
Pharmacologic classes Calcium [CS], Calcium [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base 7030 Calcium Premium
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CALCIUM .99 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination SY7Q814VUP Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 55259-1112-1 7030 Calcium Premium 120 in 1 PACKAGE CAPSULE 120 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 55259-1112 7030 CALCIUM PREMIUM (CALCIUM) CAPSULE [APEXEL CO., LTD] 2 Current NDC, 1 package rows 20240222_bdc7c833-daf7-48f9-e053-2995a90ad88e.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 55259-1112-1 55259111201 120 CAPSULE in 1 PACKAGE (55259-1112-1) 120 capsule 2021-03-18 No No Current