Home NDC 70369-005 Calcium Carbonate
Product NDC 70369-005
11-digit product format 703690005
Labeler code 70369
Product ID 70369-005_2ce809b5-d290-8c53-e063-6294a90ab784
Type HUMAN OTC DRUG
Nonproprietary name Calcium Carbonate
Dosage form TABLET
Route ORAL
Labeler CitraGen Pharmaceuticals, Inc.
Application M001
Marketing category OTC MONOGRAPH DRUG
Marketing start 2018-09-26
Substance CALCIUM CARBONATE
Active strength 1250 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 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 70369-005-03 ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 70369-005-02 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 70369-005-03 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 70369-005-02 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
Brand name suffix 1250 mg
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CALCIUM CARBONATE 1250 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 282465 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 70369-005-02 Calcium Carbonate1250 mg 500 in 1 BOTTLE TABLET 500 4 70369-005-03 Calcium Carbonate1250 mg 100 in 1 BOTTLE TABLET 100 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70369-005 CALCIUM CARBONATE 1250 MG (CALCIUM CARBONATE) TABLET [CITRAGEN PHARMACEUTICALS, INC.] 4 Current NDC, Legacy NDC, 2 package rows 20250131_766b3f3f-8bd1-281c-e053-2991aa0af54b.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 70369-005-02 70369000502 500 TABLET in 1 BOTTLE (70369-005-02) 500 tablet 2018-09-26 0000-00-00 No No Current 70369-005-03 70369000503 100 TABLET in 1 BOTTLE (70369-005-03) 100 tablet 2018-09-26 0000-00-00 No No Current