Home NDC 51645-735 Plus Pharma
Product NDC 51645-735
11-digit product format 516450735
Labeler code 51645
Product ID 51645-735_98d204ae-3e1a-bbb9-e053-2995a90afe40
Type HUMAN OTC DRUG
Nonproprietary name CALCIUM CARBONATE
Dosage form TABLET, CHEWABLE
Route ORAL
Labeler Gemini Pharmaceuticals, Inc. dba Plus Pharma
Application part331
Marketing category OTC MONOGRAPH FINAL
Marketing start 2006-03-27
Marketing end 2022-03-31
Substance CALCIUM CARBONATE
Active strength 500 mg/1
NDC exclude flag No
Listing certified through 0000-00-00
Current FDA listing Historical FDA.report record 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 · 24 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 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 51645-735-15 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 51645-735-15 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 51645-735-15 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 51645-735-15 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 51645-735-15 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 51645-735-15 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 51645-735-15 302b2466d912…e7b80fea0513…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 51645-735-15 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 51645-735-15 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 excluded product product ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 51645-735-15 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 51645-735-15 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded product product 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 51645-735-15 557ba5c1ecfa…9c80585c8c6e…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts# DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded CALCIUM CARBONATE ACTIVE INGREDIENT H0G9379FGK PLUS PHARMA CALCIUM ANTACID (CALCIUM CARBONATE) TABLET, CHEWABLE [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA ] 1 CALCIUM CATION ACTIVE MOIETY 2M83C4R6ZB PLUS PHARMA CALCIUM ANTACID (CALCIUM CARBONATE) TABLET, CHEWABLE [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA ] 1 ACACIA INACTIVE INGREDIENT 5C5403N26O PLUS PHARMA CALCIUM ANTACID (CALCIUM CARBONATE) TABLET, CHEWABLE [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA ] 1 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U PLUS PHARMA CALCIUM ANTACID (CALCIUM CARBONATE) TABLET, CHEWABLE [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA ] 1 D&C RED NO. 27 INACTIVE INGREDIENT 2LRS185U6K PLUS PHARMA CALCIUM ANTACID (CALCIUM CARBONATE) TABLET, CHEWABLE [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA ] 1 FD&C BLUE NO. 1 INACTIVE INGREDIENT H3R47K3TBD PLUS PHARMA CALCIUM ANTACID (CALCIUM CARBONATE) TABLET, CHEWABLE [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA ] 1 MAGNESIUM STEARATE INACTIVE INGREDIENT 70097M6I30 PLUS PHARMA CALCIUM ANTACID (CALCIUM CARBONATE) TABLET, CHEWABLE [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA ] 1 MALTODEXTRIN INACTIVE INGREDIENT 7CVR7L4A2D PLUS PHARMA CALCIUM ANTACID (CALCIUM CARBONATE) TABLET, CHEWABLE [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA ] 1 SILICON DIOXIDE INACTIVE INGREDIENT ETJ7Z6XBU4 PLUS PHARMA CALCIUM ANTACID (CALCIUM CARBONATE) TABLET, CHEWABLE [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA ] 1 STARCH, CORN INACTIVE INGREDIENT O8232NY3SJ PLUS PHARMA CALCIUM ANTACID (CALCIUM CARBONATE) TABLET, CHEWABLE [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA ] 1 SUCROSE INACTIVE INGREDIENT C151H8M554 PLUS PHARMA CALCIUM ANTACID (CALCIUM CARBONATE) TABLET, CHEWABLE [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA ] 1
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 51645-735-15 51645073515 150 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (51645-735-15) 2006-03-27 2022-03-31 No No Current