Home NDC 51645-850-06 Plus Pharma Senna Plus
Product NDC 51645-850
Requested package NDC 51645-850-06
11-digit product format 516450850
Labeler code 51645
Product ID 51645-850_b3db6ed6-cbc5-d23a-e053-2995a90ad052
Type HUMAN OTC DRUG
Nonproprietary name DOCUSATE SODIUM,SENNOSIDES
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 2022-03-31
Substance DOCUSATE SODIUM; SENNOSIDES
Active strength 50 mg/1; 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…
DailyMed Product Concepts# DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded DOCUSATE SODIUM ACTIVE INGREDIENT F05Q2T2JA0 PLUS PHARMA SENNA PLUS STANDARDIZED SENNA CONCENTRATE 8.6 MG AND DOCUSATE SODIUM 50 MG EACH (DOCUSATE SODIUM,SENNOSIDES) TABLET, FILM COATED [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA ] 2 SENNOSIDES ACTIVE INGREDIENT 3FYP5M0IJX PLUS PHARMA SENNA PLUS STANDARDIZED SENNA CONCENTRATE 8.6 MG AND DOCUSATE SODIUM 50 MG EACH (DOCUSATE SODIUM,SENNOSIDES) TABLET, FILM COATED [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA ] 2 DOCUSATE ACTIVE MOIETY M7P27195AG PLUS PHARMA SENNA PLUS STANDARDIZED SENNA CONCENTRATE 8.6 MG AND DOCUSATE SODIUM 50 MG EACH (DOCUSATE SODIUM,SENNOSIDES) TABLET, FILM COATED [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA ] 2 SENNOSIDES ACTIVE MOIETY 3FYP5M0IJX PLUS PHARMA SENNA PLUS STANDARDIZED SENNA CONCENTRATE 8.6 MG AND DOCUSATE SODIUM 50 MG EACH (DOCUSATE SODIUM,SENNOSIDES) TABLET, FILM COATED [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA ] 2 CALCIUM PHOSPHATE, DIBASIC, DIHYDRATE INACTIVE INGREDIENT O7TSZ97GEP PLUS PHARMA SENNA PLUS STANDARDIZED SENNA CONCENTRATE 8.6 MG AND DOCUSATE SODIUM 50 MG EACH (DOCUSATE SODIUM,SENNOSIDES) TABLET, FILM COATED [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA ] 2 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U PLUS PHARMA SENNA PLUS STANDARDIZED SENNA CONCENTRATE 8.6 MG AND DOCUSATE SODIUM 50 MG EACH (DOCUSATE SODIUM,SENNOSIDES) TABLET, FILM COATED [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA ] 2 CROSCARMELLOSE SODIUM INACTIVE INGREDIENT M28OL1HH48 PLUS PHARMA SENNA PLUS STANDARDIZED SENNA CONCENTRATE 8.6 MG AND DOCUSATE SODIUM 50 MG EACH (DOCUSATE SODIUM,SENNOSIDES) TABLET, FILM COATED [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA ] 2 D&C YELLOW NO. 10 INACTIVE INGREDIENT 35SW5USQ3G PLUS PHARMA SENNA PLUS STANDARDIZED SENNA CONCENTRATE 8.6 MG AND DOCUSATE SODIUM 50 MG EACH (DOCUSATE SODIUM,SENNOSIDES) TABLET, FILM COATED [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA ] 2 DEXTROSE INACTIVE INGREDIENT IY9XDZ35W2 PLUS PHARMA SENNA PLUS STANDARDIZED SENNA CONCENTRATE 8.6 MG AND DOCUSATE SODIUM 50 MG EACH (DOCUSATE SODIUM,SENNOSIDES) TABLET, FILM COATED [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA ] 2 FD&C YELLOW NO. 6 INACTIVE INGREDIENT H77VEI93A8 PLUS PHARMA SENNA PLUS STANDARDIZED SENNA CONCENTRATE 8.6 MG AND DOCUSATE SODIUM 50 MG EACH (DOCUSATE SODIUM,SENNOSIDES) TABLET, FILM COATED [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA ] 2 HYPROMELLOSES INACTIVE INGREDIENT 3NXW29V3WO PLUS PHARMA SENNA PLUS STANDARDIZED SENNA CONCENTRATE 8.6 MG AND DOCUSATE SODIUM 50 MG EACH (DOCUSATE SODIUM,SENNOSIDES) TABLET, FILM COATED [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA ] 2 MAGNESIUM STEARATE INACTIVE INGREDIENT 70097M6I30 PLUS PHARMA SENNA PLUS STANDARDIZED SENNA CONCENTRATE 8.6 MG AND DOCUSATE SODIUM 50 MG EACH (DOCUSATE SODIUM,SENNOSIDES) TABLET, FILM COATED [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA ] 2 POLYETHYLENE GLYCOLS INACTIVE INGREDIENT 3WJQ0SDW1A PLUS PHARMA SENNA PLUS STANDARDIZED SENNA CONCENTRATE 8.6 MG AND DOCUSATE SODIUM 50 MG EACH (DOCUSATE SODIUM,SENNOSIDES) TABLET, FILM COATED [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA ] 2 SILICON DIOXIDE INACTIVE INGREDIENT ETJ7Z6XBU4 PLUS PHARMA SENNA PLUS STANDARDIZED SENNA CONCENTRATE 8.6 MG AND DOCUSATE SODIUM 50 MG EACH (DOCUSATE SODIUM,SENNOSIDES) TABLET, FILM COATED [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA ] 2 SODIUM BENZOATE INACTIVE INGREDIENT OJ245FE5EU PLUS PHARMA SENNA PLUS STANDARDIZED SENNA CONCENTRATE 8.6 MG AND DOCUSATE SODIUM 50 MG EACH (DOCUSATE SODIUM,SENNOSIDES) TABLET, FILM COATED [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA ] 2 STEARIC ACID INACTIVE INGREDIENT 4ELV7Z65AP PLUS PHARMA SENNA PLUS STANDARDIZED SENNA CONCENTRATE 8.6 MG AND DOCUSATE SODIUM 50 MG EACH (DOCUSATE SODIUM,SENNOSIDES) TABLET, FILM COATED [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA ] 2 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP PLUS PHARMA SENNA PLUS STANDARDIZED SENNA CONCENTRATE 8.6 MG AND DOCUSATE SODIUM 50 MG EACH (DOCUSATE SODIUM,SENNOSIDES) TABLET, FILM COATED [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA ] 2
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 51645-850-06 51645085006 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51645-850-06) 2006-03-27 2022-03-31 No No Current