Home NDC 55259-0007 AG-X
Product NDC 55259-0007
11-digit product format 552590007
Labeler code 55259
Product ID 55259-0007_11cc283a-fe2c-f101-e063-6294a90ad2d4
Type HUMAN OTC DRUG
Nonproprietary name calcium
Dosage form TABLET
Route ORAL
Labeler APEXEL CO., LTD.
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2021-03-20
Substance CALCIUM
Active strength .76 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 AG-X
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CALCIUM .76 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.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 55259-0007-1 AG-X 120 in 1 BOTTLE TABLET 120 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 55259-0007 AG-X (CALCIUM) TABLET [APEXEL CO., LTD.] 3 Current NDC, Legacy NDC, 1 package rows 20240221_bdee5e24-645b-7fa0-e053-2995a90a7d25.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 Marketing end Sample Exclude flag Status 55259-0007-1 55259000701 120 TABLET in 1 BOTTLE (55259-0007-1) 120 tablet 2021-03-20 0000-00-00 No No Current