Home NDC 0280-0272 NDC 0280-0272 - Calcemin Advance This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 0280-0272
Package NDCs from labels 0280-0272-30, 0280-0272-60, 0280-0272-12
Manufacturer Bayer HealthCare LLC.
Effective date 2025-09-16
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Calcemin Advance Bayer HealthCare LLC. 2025-09-16 HUMAN OTC DRUG LABEL
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0280-0272-12 Calcemin Advance 1 in 1 CARTON TABLET, FILM COATED 1 5 0280-0272-12 Calcemin Advance 120 in 1 BOTTLE TABLET, FILM COATED 120 5 0280-0272-30 Calcemin Advance 1 in 1 CARTON TABLET, FILM COATED 1 5 0280-0272-30 Calcemin Advance 30 in 1 BOTTLE TABLET, FILM COATED 30 5 0280-0272-60 Calcemin Advance 60 in 1 BOTTLE TABLET, FILM COATED 60 5 0280-0272-60 Calcemin Advance 1 in 1 CARTON TABLET, FILM COATED 1 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0280-0272 CALCEMIN ADVANCE (CALCIUM CITRATE) TABLET, FILM COATED [BAYER HEALTHCARE LLC.] 3 6 package rows 20200529_3161469e-6402-607a-e054-00144ff88e88.zip