FDA.reportPublic FDA data

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Product NDC
70677-0080
Requested package NDC
70677-0080-1
11-digit product format
706770080
Labeler code
70677
Product ID
70677-0080_b1e57dfc-34ec-4fd6-8696-df2bf76b9b0a
Type
HUMAN OTC DRUG
Nonproprietary name
DOCUSATE CALCIUM
Dosage form
CAPSULE, LIQUID FILLED
Route
ORAL
Labeler
Strategic Sourcing Services LLC
Application
part334
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2019-11-29
Marketing end
0000-00-00
Substance
DOCUSATE CALCIUM
Active strength
240 mg/1
NDC exclude flag
No
Listing certified through
2023-12-31
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 packagepackage70677-008070677-0080-1DDiscontinued by firm2026-07-31

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
70677-0080-1706770080011 BOTTLE, PLASTIC in 1 BOX (70677-0080-1) > 100 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC2019-11-290000-00-00NoNoCurrent