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Product NDC 17433-9884
11-digit product format 174339884
Labeler code 17433
Product ID 17433-9884_ecfb2ef6-2401-52c5-e053-2995a90a4ff6
Type HUMAN OTC DRUG
Nonproprietary name docusate sodium
Dosage form LIQUID
Route RECTAL
Labeler Enemeez LLC DBA Summit Pharmaceuticals
Application part334
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2014-01-14
Marketing end 0000-00-00
Substance DOCUSATE SODIUM
Active strength 100 mg/5mL
NDC exclude flag No
Listing certified through 2023-12-31
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 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product 17433-9884 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 17433-9884 17433-9884-5 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 17433-9884 DOCUSOL KIDS (DOCUSATE SODIUM) LIQUID [ENEMEEZ LLC DBA SUMMIT PHARMACEUTICALS] 8 Legacy NDC 20230115_0d9355f0-d19f-4404-9b9e-bb2c874e39d6.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 17433-9884-5 17433988405 5 TUBE in 1 BOX (17433-9884-5) > 5 mL in 1 TUBE (17433-9884-1) 5 tube 2014-01-14 0000-00-00 No No Current