Home NDC 0904-7889-80 MAJOR DOK Docusate Sodium
Product NDC 0904-7889
Requested package NDC 0904-7889-80
11-digit product format 009047889
Labeler code 0904
Product ID 0904-7889_0a365519-8f0a-4f1f-80b7-a7f1b3022033
Type HUMAN OTC DRUG
Nonproprietary name DOCUSATE SODIUM
Dosage form CAPSULE, LIQUID FILLED
Route ORAL
Labeler Major Pharmaceuticals
Application part334
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2010-04-23
Marketing end 2021-12-30
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 DOCUSATE SODIUM CAPSULE, LIQUID FILLED [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS] 7 DOCUSATE ACTIVE MOIETY M7P27195AG DOCUSATE SODIUM CAPSULE, LIQUID FILLED [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS] 7 FD&C RED NO. 40 INACTIVE INGREDIENT WZB9127XOA DOCUSATE SODIUM CAPSULE, LIQUID FILLED [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS] 7 FD&C YELLOW NO. 6 INACTIVE INGREDIENT H77VEI93A8 DOCUSATE SODIUM CAPSULE, LIQUID FILLED [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS] 7 GELATIN INACTIVE INGREDIENT 2G86QN327L DOCUSATE SODIUM CAPSULE, LIQUID FILLED [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS] 7 GLYCERIN INACTIVE INGREDIENT PDC6A3C0OX DOCUSATE SODIUM CAPSULE, LIQUID FILLED [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS] 7 POLYETHYLENE GLYCOLS INACTIVE INGREDIENT 3WJQ0SDW1A DOCUSATE SODIUM CAPSULE, LIQUID FILLED [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS] 7 PROPYLENE GLYCOL INACTIVE INGREDIENT 6DC9Q167V3 DOCUSATE SODIUM CAPSULE, LIQUID FILLED [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS] 7 SORBITOL INACTIVE INGREDIENT 506T60A25R DOCUSATE SODIUM CAPSULE, LIQUID FILLED [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS] 7 WATER INACTIVE INGREDIENT 059QF0KO0R DOCUSATE SODIUM CAPSULE, LIQUID FILLED [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS] 7 DOCUSATE SODIUM ACTIVE INGREDIENT F05Q2T2JA0 MAJOR DOK DOCUSATE SODIUM (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [MAJOR PHARMACEUTICALS] 2 DOCUSATE ACTIVE MOIETY M7P27195AG MAJOR DOK DOCUSATE SODIUM (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [MAJOR PHARMACEUTICALS] 2 FD&C RED NO. 40 INACTIVE INGREDIENT WZB9127XOA MAJOR DOK DOCUSATE SODIUM (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [MAJOR PHARMACEUTICALS] 2 FD&C YELLOW NO. 6 INACTIVE INGREDIENT H77VEI93A8 MAJOR DOK DOCUSATE SODIUM (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [MAJOR PHARMACEUTICALS] 2 GELATIN INACTIVE INGREDIENT 2G86QN327L MAJOR DOK DOCUSATE SODIUM (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [MAJOR PHARMACEUTICALS] 2 GLYCERIN INACTIVE INGREDIENT PDC6A3C0OX MAJOR DOK DOCUSATE SODIUM (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [MAJOR PHARMACEUTICALS] 2 POLYETHYLENE GLYCOLS INACTIVE INGREDIENT 3WJQ0SDW1A MAJOR DOK DOCUSATE SODIUM (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [MAJOR PHARMACEUTICALS] 2 PROPYLENE GLYCOL INACTIVE INGREDIENT 6DC9Q167V3 MAJOR DOK DOCUSATE SODIUM (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [MAJOR PHARMACEUTICALS] 2 SORBITOL INACTIVE INGREDIENT 506T60A25R MAJOR DOK DOCUSATE SODIUM (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [MAJOR PHARMACEUTICALS] 2 WATER INACTIVE INGREDIENT 059QF0KO0R MAJOR DOK DOCUSATE SODIUM (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [MAJOR PHARMACEUTICALS] 2 DOCUSATE SODIUM ACTIVE INGREDIENT F05Q2T2JA0 DOCUSATE SODIUM CAPSULE, LIQUID FILLED [CONTRACT PHARMACY SERVICES-PA] 1 DOCUSATE ACTIVE MOIETY M7P27195AG DOCUSATE SODIUM CAPSULE, LIQUID FILLED [CONTRACT PHARMACY SERVICES-PA] 1
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 0904-7889-80 00904788980 1000 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (0904-7889-80) 2010-04-23 2021-12-30 No No Current