FDA.reportPublic FDA data

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Product NDC
70518-3013
Requested package NDC
70518-3013-0
11-digit product format
705183013
Labeler code
70518
Product ID
70518-3013_d3d11ef8-b03b-2b60-e053-2995a90a212e
Type
HUMAN OTC DRUG
Nonproprietary name
Docusate calcium
Dosage form
CAPSULE, LIQUID FILLED
Route
ORAL
Labeler
REMEDYREPACK INC.
Application
part334
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2021-02-02
Marketing end
0000-00-00
Substance
DOCUSATE CALCIUM
Active strength
240 mg/1
NDC exclude flag
No
Listing certified through
2022-12-31
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 packagepackage70518-301370518-3013-0DDiscontinued by firm2026-07-31

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70518-3013-02023-10-16C16284748780-1f386c649-99e1-0266-e053-dadaa90a7c1aDrug Facts
70518-3013-02023-01-30C16284748780-1f386c649-99e1-0266-e053-dadaa90a7c1aDrug Facts

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70518-3013-070518301300100 POUCH in 1 BOX (70518-3013-0) > 1 CAPSULE, LIQUID FILLED in 1 POUCH (70518-3013-1) 100 pouch2021-02-020000-00-00NoNoCurrent