Home NDC 51013-323 Extra Strength Antacid
Product NDC 51013-323
11-digit product format 510130323
Labeler code 51013
Product ID 51013-323_5f8ca325-03d7-4046-ad97-44e43e970a91
Type HUMAN OTC DRUG
Nonproprietary name Calcium Carbonate
Dosage form TABLET, CHEWABLE
Route ORAL
Labeler PuraCap Pharmaceutical LLC
Application part331
Marketing category OTC MONOGRAPH FINAL
Marketing start 2017-12-13
Substance CALCIUM CARBONATE
Active strength 750 mg/1
Pharmacologic classes Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Extra Strength Antacid
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CALCIUM CARBONATE 750 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 308915 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 51013-323-54 Extra Strength Antacid 15 in 1 CARTON TABLET, CHEWABLE 15 1 51013-323-54 Extra Strength Antacid 2 in 1 POUCH TABLET, CHEWABLE 2 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 51013-323 EXTRA STRENGTH ANTACID (CALCIUM CARBONATE) TABLET, CHEWABLE [PURACAP PHARMACEUTICAL LLC] 1 Current NDC, Legacy NDC, 2 package rows 20171214_80509620-a3d1-49d5-b2e3-bff61ef4583d.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 Units Marketing start Marketing end Sample Exclude flag Status 51013-323-54 51013032354 15 POUCH in 1 CARTON (51013-323-54) / 2 TABLET, CHEWABLE in 1 POUCH 15 pouch 2017-12-13 0000-00-00 No No Current