Home NDC 73057-377 Calcium Carbonate 10 gr (648 mg)
Product NDC 73057-377
11-digit product format 730570377
Labeler code 73057
Product ID 73057-377_2c2a5a1c-0aa7-6253-e063-6294a90a6b5a
Type HUMAN OTC DRUG
Nonproprietary name Calcium Carbonate 10gr (648 mg)
Dosage form TABLET
Route ORAL
Labeler Ulai Health LLC
Application M001
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-07-01
Substance CALCIUM CARBONATE
Active strength 648 mg/1
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 6 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-01-20 13:05 UTC · source 2025-01-20 excluded product product ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 73057-377-11 ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 73057-377-08 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 73057-377-11 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 73057-377-08 0efc9e666f02…f202fb6c5f17…
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 Calcium Carbonate 10 gr (648 mg)
Brand name suffix (Antacid)
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CALCIUM CARBONATE 648 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination H0G9379FGK Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 577040 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 73057-377-08 Calcium Carbonate 10 gr (648 mg)(Antacid) 100 in 1 BOTTLE, PLASTIC TABLET 100 3 73057-377-11 Calcium Carbonate 10 gr (648 mg)(Antacid) 1000 in 1 BOTTLE, PLASTIC TABLET 1000 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 73057-377 CALCIUM CARBONATE 10 GR (648 MG) (ANTACID) (CALCIUM CARBONATE 10GR (648 MG)) TABLET [ULAI HEALTH LLC] 3 Current NDC, Legacy NDC, 2 package rows 20250122_641ae5b9-3bb6-41a1-ab12-367bf2fbcb0a.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 Units Marketing start Marketing end Sample Exclude flag Status 73057-377-08 73057037708 100 TABLET in 1 BOTTLE, PLASTIC (73057-377-08) 100 tablet 2019-07-01 0000-00-00 No No Current 73057-377-11 73057037711 1000 TABLET in 1 BOTTLE, PLASTIC (73057-377-11) 1000 tablet 2019-07-01 0000-00-00 No No Current