Home NDC 51645-750-10 PlusPHARMA
Product NDC 51645-750
Requested package NDC 51645-750-10
11-digit product format 516450750
Labeler code 51645
Product ID 51645-750_b3db5c6e-199b-d0ec-e053-2995a90a968c
Type HUMAN OTC DRUG
Nonproprietary name DOCUSATE SODIUM
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Gemini Pharmaceuticals, Inc. dba Plus Pharma
Application part334
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2006-03-27
Marketing end 2021-11-30
Substance DOCUSATE SODIUM
Active strength 100 mg/1
NDC exclude flag No
Listing certified through 0000-00-00
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 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded DOCUSATE SODIUM ACTIVE INGREDIENT F05Q2T2JA0 PLUSPHARMA STOOL SOFTENER (DOCUSATE SODIUM) TABLET, FILM COATED [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA] 5 DOCUSATE ACTIVE MOIETY M7P27195AG PLUSPHARMA STOOL SOFTENER (DOCUSATE SODIUM) TABLET, FILM COATED [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA] 5 CALCIUM PHOSPHATE, DIBASIC, DIHYDRATE INACTIVE INGREDIENT O7TSZ97GEP PLUSPHARMA STOOL SOFTENER (DOCUSATE SODIUM) TABLET, FILM COATED [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA] 5 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U PLUSPHARMA STOOL SOFTENER (DOCUSATE SODIUM) TABLET, FILM COATED [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA] 5 CROSCARMELLOSE SODIUM INACTIVE INGREDIENT M28OL1HH48 PLUSPHARMA STOOL SOFTENER (DOCUSATE SODIUM) TABLET, FILM COATED [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA] 5 HYPROMELLOSES INACTIVE INGREDIENT 3NXW29V3WO PLUSPHARMA STOOL SOFTENER (DOCUSATE SODIUM) TABLET, FILM COATED [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA] 5 MAGNESIUM STEARATE INACTIVE INGREDIENT 70097M6I30 PLUSPHARMA STOOL SOFTENER (DOCUSATE SODIUM) TABLET, FILM COATED [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA] 5 POLYETHYLENE GLYCOLS INACTIVE INGREDIENT 3WJQ0SDW1A PLUSPHARMA STOOL SOFTENER (DOCUSATE SODIUM) TABLET, FILM COATED [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA] 5 SILICON DIOXIDE INACTIVE INGREDIENT ETJ7Z6XBU4 PLUSPHARMA STOOL SOFTENER (DOCUSATE SODIUM) TABLET, FILM COATED [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA] 5 SODIUM BENZOATE INACTIVE INGREDIENT OJ245FE5EU PLUSPHARMA STOOL SOFTENER (DOCUSATE SODIUM) TABLET, FILM COATED [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA] 5 STARCH, CORN INACTIVE INGREDIENT O8232NY3SJ PLUSPHARMA STOOL SOFTENER (DOCUSATE SODIUM) TABLET, FILM COATED [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA] 5 STEARIC ACID INACTIVE INGREDIENT 4ELV7Z65AP PLUSPHARMA STOOL SOFTENER (DOCUSATE SODIUM) TABLET, FILM COATED [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA] 5
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 51645-750-10 51645075010 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51645-750-10) 2006-03-27 2021-11-30 No No Current