EZ2go

Product NDC
76470-011
11-digit product format
764700011
Labeler code
76470
Product ID
76470-011_af0e7c58-db2a-337c-e053-2995a90a8be2
Type
HUMAN OTC DRUG
Nonproprietary name
Bisacodyl
Dosage form
PILL
Route
ORAL
Labeler
Valley Medical Products,LLC
Application
part334
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2015-01-01
Marketing end
0000-00-00
Substance
BISACODYL
Active strength
5 mg/5mg
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct76470-011DDiscontinued by firm2026-10-05
excluded packagepackage76470-01176470-011-11DDiscontinued by firm2026-10-05

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 · 24 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded productproductd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage76470-011-11d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded productproductf5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage76470-011-11f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-31excluded productproduct2ef7874e63bc…57b86245f4fa…
2025-04-01 02:39 UTC · source 2025-03-31excluded packagepackage76470-011-112ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28excluded productproducta1b67e2a42f9…c4cf2c586c0d…
2025-03-28 20:22 UTC · source 2025-03-28excluded packagepackage76470-011-11a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21excluded productproductcfe11265f3b6…090c488252e2…
2025-03-22 03:12 UTC · source 2025-03-21excluded packagepackage76470-011-11cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10excluded productproductcdf11ea48f46…ba0047e9e063…
2025-03-10 12:48 UTC · source 2025-03-10excluded packagepackage76470-011-11cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31excluded productproduct302b2466d912…e7b80fea0513…
2025-02-02 03:52 UTC · source 2025-01-31excluded packagepackage76470-011-11302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20excluded productproducted331223b511…672a5bd82f5f…
2025-01-20 13:05 UTC · source 2025-01-20excluded packagepackage76470-011-11ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-10excluded productproduct0efc9e666f02…f202fb6c5f17…
2025-01-11 03:41 UTC · source 2025-01-10excluded packagepackage76470-011-110efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08excluded productproductad56d346431e…cc804d4bbf1e…
2024-11-09 02:27 UTC · source 2024-11-08excluded packagepackage76470-011-11ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03excluded productproduct367a005e9d99…383a685ebd0f…
2024-10-04 04:10 UTC · source 2024-10-03excluded packagepackage76470-011-11367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09excluded productproduct557ba5c1ecfa…9c80585c8c6e…
2024-07-10 04:00 UTC · source 2024-07-09excluded packagepackage76470-011-11557ba5c1ecfa…9c80585c8c6e…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
BisacodylACTIVE INGREDIENT10X0709Y6IEZ2GO (BISACODYL) PILL [VALLEY MEDICAL PRODUCTS,LLC]1
BisacodylACTIVE MOIETY10X0709Y6IEZ2GO (BISACODYL) PILL [VALLEY MEDICAL PRODUCTS,LLC]1
CALCIUM CARBONATEINACTIVE INGREDIENTH0G9379FGKEZ2GO (BISACODYL) PILL [VALLEY MEDICAL PRODUCTS,LLC]1
CALCIUM PHOSPHATE, DIBASIC, ANHYDROUSINACTIVE INGREDIENTL11K75P92JEZ2GO (BISACODYL) PILL [VALLEY MEDICAL PRODUCTS,LLC]1
CARNAUBA WAXINACTIVE INGREDIENTR12CBM0EIZEZ2GO (BISACODYL) PILL [VALLEY MEDICAL PRODUCTS,LLC]1
CROSCARMELLOSE SODIUMINACTIVE INGREDIENTM28OL1HH48EZ2GO (BISACODYL) PILL [VALLEY MEDICAL PRODUCTS,LLC]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30EZ2GO (BISACODYL) PILL [VALLEY MEDICAL PRODUCTS,LLC]1
MALTODEXTRININACTIVE INGREDIENT7CVR7L4A2DEZ2GO (BISACODYL) PILL [VALLEY MEDICAL PRODUCTS,LLC]1
POWDERED CELLULOSEINACTIVE INGREDIENTSMD1X3XO9MEZ2GO (BISACODYL) PILL [VALLEY MEDICAL PRODUCTS,LLC]1
SHELLACINACTIVE INGREDIENT46N107B71OEZ2GO (BISACODYL) PILL [VALLEY MEDICAL PRODUCTS,LLC]1
SILICON DIOXIDEINACTIVE INGREDIENTETJ7Z6XBU4EZ2GO (BISACODYL) PILL [VALLEY MEDICAL PRODUCTS,LLC]1
STEARIC ACIDINACTIVE INGREDIENT4ELV7Z65APEZ2GO (BISACODYL) PILL [VALLEY MEDICAL PRODUCTS,LLC]1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
76470-011-117647000111120 mg in 1 BOTTLE (76470-011-11) 20 mg2015-01-010000-00-00NoNoCurrent