Home NDC 72789-166-60 Docusate Sodium
Product NDC 72789-166
Requested package NDC 72789-166-60
11-digit product format 727890166
Labeler code 72789
Product ID 72789-166_5df8220e-553c-a533-e063-6394a90a4269
Type HUMAN OTC DRUG
Nonproprietary name Docusate Sodium
Dosage form CAPSULE, LIQUID FILLED
Route ORAL
Labeler PD-Rx Pharmaceuticals, Inc.
Application M007
Marketing category OTC MONOGRAPH DRUG
Marketing start 2000-05-01
Marketing end 2027-10-31
Substance DOCUSATE SODIUM
Active strength 250 mg/1
NDC exclude flag No
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Docusate Sodium Active Ingredients# Ingredient, Strength table Ingredient Strength DOCUSATE SODIUM 250 mg/1
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72789-166-60 Docusate Sodium 60 in 1 BOTTLE, PLASTIC CAPSULE, LIQUID FILLED 60 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72789-166 DOCUSATE SODIUM CAPSULE, LIQUID FILLED [PD-RX PHARMACEUTICALS, INC.] 6 Current NDC, Legacy NDC, 1 package rows 20250207_6a7e4193-22d2-491e-9842-5c43f571fc65.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 14 of 42 · 829 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 72789-166-60 72789016660 60 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (72789-166-60) 2021-02-10 2027-10-31 No No Current