FDA.reportPublic FDA data

ANTACID REGULAR STRENGTH

Product NDC
70692-118
Requested package NDC
70692-118-45
11-digit product format
706920118
Labeler code
70692
Product ID
70692-118_b1a796db-91d0-a8a7-e053-2a95a90a67df
Type
HUMAN OTC DRUG
Nonproprietary name
Calcium Carbonate 500mg
Dosage form
TABLET, CHEWABLE
Route
ORAL
Labeler
Strive Pharmaceuticals Inc.
Application
part331
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2018-05-09
Marketing end
0000-00-00
Substance
CALCIUM CARBONATE
Active strength
500 mg/1
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

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

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage70692-11870692-118-45IInactivated by FDA2026-07-31

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
bee4fa8d-8d82-423a-a0b5-40a89dd13a99Product name120250618
e0d2eb29-08bd-4bba-90d1-c91c68a38767Product name420250516
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
334fe8d2-68fb-4331-a576-420e302ec069Product name720240320
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
e92765c1-be81-432a-b909-1b10777ec378Product name120190208
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
0441a8f5-3835-497c-aedd-bc78cba56b2aProduct name120150317
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70692-118-452022-01-28C16284748780-1d6a99b39-6318-a426-e053-dadaa90af4c2ANATACID REGULAR STRENGTH Calcium Carbonate 500mg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70692-118-45ANTACID REGULAR STRENGTH45 in 1 PACKAGETABLET, CHEWABLE453

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70692-118ANTACID REGULAR STRENGTH (CALCIUM CARBONATE 500MG) TABLET, CHEWABLE [STRIVE PHARMACEUTICALS INC.]3Legacy NDC, 1 package rows20201015_6bcadbc0-2d5d-5d75-e053-2991aa0a1c2a.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
308907calcium carbonate 500 MG (Ca 200 MG) Chewable TabletPSN6bcadbc0-2d5d-5d75-e053-2991aa0a1c2a3
308907calcium carbonate 500 MG Chewable TabletSCD6bcadbc0-2d5d-5d75-e053-2991aa0a1c2a3
308907calcium carbonate 500 MG (equivalent to calcium 200 MG) Chewable TabletSY6bcadbc0-2d5d-5d75-e053-2991aa0a1c2a3

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
70692-118-457069201184545 TABLET, CHEWABLE in 1 PACKAGE (70692-118-45) 2018-05-090000-00-00NoNoCurrent