Home NDC 68998-103 Marc Glassman
Product NDC 68998-103
11-digit product format 689980103
Labeler code 68998
Product ID 68998-103_066b8430-87a4-4f73-8e12-e19bf4e91e46
Type HUMAN OTC DRUG
Nonproprietary name Calcium Carbonate
Dosage form TABLET, CHEWABLE
Route ORAL
Labeler MARC GLASSMAN, INC
Application M001
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-04-17
Substance CALCIUM CARBONATE
Active strength 1000 mg/1
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Marc Glassman
Brand name suffix Ultra Strength
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CALCIUM CARBONATE 1000 mg/1
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 68998-103-72 Marc GlassmanUltra Strength 72 in 1 BOTTLE, PLASTIC TABLET, CHEWABLE 72 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68998-103 MARC GLASSMAN ULTRA STRENGTH (CALCIUM CARBONATE) TABLET, CHEWABLE [MARC GLASSMAN, INC] 7 Current NDC, Legacy NDC, 1 package rows 20241010_35372a73-9578-4f46-9005-019fd8dd2e18.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 8 of 34 · 678 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 68998-103-72 68998010372 72 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (68998-103-72) 2019-04-17 0000-00-00 No No Current