DGH Antacid Regular Strength 500 (Fruit assorted), 150ct

Product NDC
71481-003
Requested package NDC
71481-003-01
11-digit product format
714810003
Labeler code
71481
Product ID
71481-003_d955e516-5459-1b07-e053-2a95a90aa6d9
Type
HUMAN OTC DRUG
Nonproprietary name
CALCIUM CARBONATE
Dosage form
TABLET
Route
ORAL
Labeler
BioV Health Inc
Application
part331
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2022-02-28
Marketing end
0000-00-00
Substance
CALCIUM CARBONATE
Active strength
500 mg/1
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage71481-00371481-003-01IInactivated by FDA2026-10-15

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 · 3 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage71481-00371481-003-01IInactivated by FDAexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage71481-00371481-003-01IInactivated by FDAexcluded / ndc_excluded.zipf5e01cc5f278…a2eaf40c39c3…
2024-03-11 06:39 UTC · source 2024-03-08excluded packagepackage71481-00371481-003-01IInactivated by FDAexcluded / ndc_excluded.zip1332a3947898…d4bfe170f9cd…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71481-003-01DGH Antacid Regular Strength 500 (Fruit assorted), 150ct150 in 1 BOTTLETABLET1502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71481-003DGH ANTACID REGULAR STRENGTH 500 (FRUIT ASSORTED), 150CT (CALCIUM CARBONATE) TABLET [BIOV HEALTH INC]2Legacy NDC, 1 package rows20240405_3a8adf74-a15d-4ca6-8eba-1a4b2f5d41e0.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
308907calcium carbonate 500 MG (Ca 200 MG) Chewable TabletPSN3a8adf74-a15d-4ca6-8eba-1a4b2f5d41e02
308907calcium carbonate 500 MG Chewable TabletSCD3a8adf74-a15d-4ca6-8eba-1a4b2f5d41e02
308907calcium carbonate 500 MG (equivalent to calcium 200 MG) Chewable TabletSY3a8adf74-a15d-4ca6-8eba-1a4b2f5d41e02

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71481-003-0171481000301150 TABLET in 1 BOTTLE (71481-003-01) 150 tablet2022-02-280000-00-00NoNoCurrent