Home NDC 24385-478 Regular Strength Antacid
Product NDC 24385-478
11-digit product format 243850478
Labeler code 24385
Product ID 24385-478_e02b82af-ac4b-42b3-a9a3-c2ac316ea062
Type HUMAN OTC DRUG
Nonproprietary name Calcium carbonate
Dosage form TABLET, CHEWABLE
Route ORAL
Labeler Amerisource Bergen
Application part331
Marketing category OTC MONOGRAPH DRUG
Marketing start 2016-10-31
Substance CALCIUM CARBONATE
Active strength 500 mg/1
Pharmacologic classes Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA]
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 2024-05-28 21:12 UTC · source 2024-05-28 excluded product product 8af77b9d5b6f…d9bbb34c5368…2024-05-28 21:12 UTC · source 2024-05-28 excluded package package 24385-478-47 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 excluded product product 834df4deac94…adcc014656a3…2024-05-15 03:39 UTC · source 2024-05-14 excluded package package 24385-478-47 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 excluded product product 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 24385-478-47 1332a3947898…d4bfe170f9cd…
Additional Listing Data#
Finished product Yes
Brand name base Regular Strength Antacid
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CALCIUM CARBONATE 500 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 308907 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 24385-478-47 Regular Strength Antacid 150 in 1 BOTTLE TABLET, CHEWABLE 150 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 24385-478 REGULAR STRENGTH ANTACID (CALCIUM CARBONATE) TABLET, CHEWABLE [AMERISOURCE BERGEN] 2 Current NDC, Legacy NDC, 1 package rows 20240629_f9dd2797-c804-43c4-9d64-47de3b63a19a.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.
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 24385-478-47 24385047847 150 TABLET, CHEWABLE in 1 BOTTLE (24385-478-47) 2016-10-31 0000-00-00 No No Current